Tag mr [at least 200 articles] Export

Recent papers classified by the tag mr.

	Lessons learnt from large-scale exon re-sequencing of the X chromosome. [My Copy] Human molecular genetics, Vol. 18, No. R1. (15 April 2009) by F. Lucy Raymond, Annabel Whibley, Michael R. Stratton, Jozef Gecz posted to synaptic nssnps mr genomics by daforerog on 2009-11-18 17:10:57 as along with 1 person jdbowes
	A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation [My Copy] Nature Genetics, Vol. 41, No. 5. (19 April 2009), pp. 535-543. by Patrick S. Tarpey, Raffaella Smith, Erin Pleasance, et al.Annabel Whibley, Sarah Edkins, Claire Hardy, Sarah O'Meara, Calli Latimer, Ed Dicks, Andrew Menzies, Phil Stephens, Matt Blow, Chris Greenman, Yali Xue, Chris Tyler-Smith, Deborah Thompson, Kristian Gray, Jenny Andrews, Syd Barthorpe, Gemma Buck, Jennifer Cole, Rebecca Dunmore, David Jones, Mark Maddison, Tatiana Mironenko, Rachel Turner, Kelly Turrell, Jennifer Varian, Sofie West, Sara Widaa, Paul Wray, Jon Teague, Adam Butler, Andrew Jenkinson, Mingming Jia, David Richardson, Rebecca Shepherd, Richard Wooster, M. Isabel Tejada, Francisco Martinez, Gemma Carvill, Rene Goliath, Arjan P. M. de Brouwer, Hans van Bokhoven, Hilde Van Esch, Jamel Chelly, Martine Raynaud, Hans-Hilger Ropers, Fatima E. Abidi, Anand K. Srivastava, James Cox, Ying Luo, Uma Mallya, Jenny Moon, Josef Parnau, Shehla Mohammed, John L. Tolmie, Cheryl Shoubridge, Mark Corbett, Alison Gardner, Eric Haan, Sinitdhorn Rujirabanjerd, Marie Shaw, Lucianne Vandeleur, Tod Fullston, Douglas F. Easton, Jackie Boyle, Michael Partington, Anna Hackett, Michael Field, Cindy Skinner, Roger E. Stevenson, Martin Bobrow, Gillian Turner, Charles E. Schwartz, Jozef Gecz, F. Lucy Raymond, P. Andrew Futreal, Michael R. Stratton posted to sequencing mr by vplagnol on 2009-11-13 11:49:11 as along with 5 people and 2 groups Peiyong avilella jandot fenghezi daforerog Ensembl Compara citations Journal picks
	A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. [My Copy] Nature genetics (8 November 2009) by Marwan Shinawi, Christian P. Schaaf, Samarth S. Bhatt, et al.Zhilian Xia, Ankita Patel, Sau Wai W. Cheung, Brendan Lanpher, Sandra Nagl, Heinrich Stephan S. Herding, Claudia Nevinny-Stickel, Ladonna L. Immken, Gayle Simpson S. Patel, Jennifer Ruth R. German, Arthur L. Beaudet, Pawel Stankiewicz posted to psychgen mr cnv by daforerog on 2009-11-12 15:49:43 as
	Chromosome 21-derived mirnas provide an etiological basis for aberrant protein expression in human down syndrome brains. [My Copy] The Journal of biological chemistry (6 November 2009) by Donald E. Kuhn, Gerard J. Nuovo, Alvin V. Terry, et al.Mickey M. Martin, Geraldine E. Malana, Sarah E. Sansom, Adam P. Pleister, Wayne D. Beck, Elizabeth Head, David S. Feldman, Terry S. Elton posted to mr mirna find by daforerog on 2009-11-12 15:48:53 as
	CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila. [My Copy] American journal of human genetics (4 November 2009) by Christiane Zweier, Eiko K. de Jong, Markus Zweier, et al.Alfredo Orrico, Lilian B. Ousager, Amanda L. Collins, Emilia K. Bijlsma, Merel A. Oortveld, Arif B. Ekici, André Reis, Annette Schenck, Anita Rauch posted to synaptic mr brainmut by daforerog on 2009-11-12 09:13:08 as
	Method to correct intensity inhomogeneity in MR images for atherosclerosis characterization [My Copy] Medical Imaging, IEEE Transactions on, Vol. 25, No. 5. (01 May 2006), pp. 539-552. by O. Salvado, C. Hillenbrand, Shaoxiang Zhang, D. L. Wilson posted to mr bias_field by robertmarti on 2009-11-04 16:32:25 as
	Modeling of contrast agent kinetics in the lung using <I>T</I><SUB><FONT SIZE='-1'>1</FONT></SUB>-weighted dynamic contrast-enhanced MRI [My Copy] Magnetic Resonance in Medicine, Vol. 61, No. 6. (2009), pp. 1507-1514. by Josephine H. Naish, Lucy E. Kershaw, David L. Buckley, Alan Jackson, John C. Waterton, Geoffrey J. M. Parker posted to mr lung dce akaike by anitabanerji on 2009-10-27 11:11:25 as
	Pharmacokinetic analysis of tissue microcirculation using nested models: multimodel inference and parameter identifiability. [My Copy] Medical physics, Vol. 36, No. 7. (July 2009), pp. 2923-2933. by Gunnar Brix, Stefan Zwick, Fabian Kiessling, Jürgen Griebel posted to pharmokinetic-model mr dce akaike by anitabanerji on 2009-10-27 10:50:01 as
	Universal spin-induced magnetoresistance in the variable-range hopping regime [My Copy] EPL (Europhysics Letters), Vol. 33, No. 6. (1996), pp. 471-476. by Y. Meir posted to vrh quantum_interference_effects mr by vagantes on 2009-10-14 18:01:10 as
	A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation [My Copy] neurogenetics by Ginevra Zanni, Hilde van Esch, Anissa Bensalem, et al.Yoann Saillour, Karine Poirier, Laetitia Castelnau, Hans Ropers, Arjan de Brouwer, Fréderic Laumonnier, Jean-Pierre Fryns, Jamel Chelly posted to synaptic nssnps mr humgen by daforerog on 2009-10-02 11:52:28 as
	Handbook of MRI Pulse Sequences [My Copy] (21 September 2004) by Matt A. Bernstein, Kevin F. King, Xiaohong J. Zhou posted to sequence mr by ctoraci on 2009-09-21 17:09:51 as along with 8 people and 2 groups Aolty jsyu01 mbolding xtizon vanzaj anitabanerji ppxom co8 Functional_Imaging Neuroscience
	Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study. [My Copy] Brain : a journal of neurology (15 September 2009) by Raffaele Lodi, Piero Parchi, Caterina Tonon, et al.David Manners, Sabina Capellari, Rosaria Strammiello, Rita Rinaldi, Claudia Testa, Emil Malucelli, Barbara Mostacci, Giovanni Rizzo, Giulia Pierangeli, Pietro Cortelli, Pasquale Montagna, Bruno Barbiroli posted to study sporadic spectroscopy pd mr markers diagnostics clinical by calvin on 2009-09-18 21:07:09 as along with 1 person applebyb
	Clinical and Benefit--Cost Outcomes of Teaching a Mindfulness-Based Procedure to Adult Offenders With Intellectual Disabilities [My Copy] Behav Modif, Vol. 32, No. 5. (1 September 2008), pp. 622-637. by Nirbhay N. Singh, Giulio E. Lancioni, Alan S. W. Winton, Ashvind N. Singh, Angela D. Adkins, Judy Singh posted to therapy offender mr mindfulness case-reports by jfpsy to the group Clinical_Psychology on 2009-09-15 08:17:05 as
	Treatment of Chronic Skin-Picking in an Adolescent With Asperger Syndrome and Borderline Intellectual Disability [My Copy] Clinical Case Studies, Vol. 8, No. 4. (1 August 2009), pp. 317-325. by Russell Lang, Robert Didden, Jeff Sigafoos, Mandy Rispoli, April Regester, Giulio E. Lancioni posted to therapy skin-picking mr case-reports autism adolescence by jfpsy to the group Clinical_Psychology on 2009-09-15 07:18:56 as
	Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome. [My Copy] Journal of medical genetics, Vol. 46, No. 7. (July 2009), pp. 480-489. by T. Y. Tan, S. Aftimos, L. Worgan, et al.R. Susman, M. Wilson, S. Ghedia, E. P. Kirk, D. Love, A. Ronan, A. Darmanian, A. Slavotinek, J. Hogue, J. B. Moeschler, J. Ozmore, R. Widmer, R. Savarirayan, G. Peters posted to mr humgen genomics cnv by daforerog on 2009-09-14 17:04:11 as
	Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. [My Copy] Journal of medical genetics, Vol. 45, No. 11. (November 2008), pp. 710-720. by D. A. Koolen, A. J. Sharp, J. A. Hurst, et al.H. V. Firth, S. J. Knight, A. Goldenberg, P. Saugier-Veber, R. Pfundt, L. E. Vissers, A. Destrée, B. Grisart, L. Rooms, N. Van der Aa, M. Field, A. Hackett, K. Bell, M. J. Nowaczyk, G. M. Mancini, P. J. Poddighe, C. E. Schwartz, E. Rossi, M. De Gregori, L. L. Antonacci-Fulton, M. D. McLellan, J. M. Garrett, M. A. Wiechert, T. L. Miner, S. Crosby, R. Ciccone, L. Willatt, A. Rauch, M. Zenker, S. Aradhya, M. A. Manning, T. M. Strom, J. Wagenstaller, A. C. Krepischi-Santos, A. M. Vianna-Morgante, C. Rosenberg, S. M. Price, H. Stewart, C. Shaw-Smith, H. G. Brunner, A. O. Wilkie, J. A. Veltman, O. Zuffardi, E. E. Eichler, B. B. de Vries posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:59:40 as
	A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. [My Copy] Nature genetics, Vol. 38, No. 9. (13 September 2006), pp. 999-1001. by David A. Koolen, Lisenka E. Vissers, Rolph Pfundt, et al.Nicole de Leeuw, Samantha J. Knight, Regina Regan, R. Frank Kooy, Edwin Reyniers, Corrado Romano, Marco Fichera, Albert Schinzel, Alessandra Baumer, Britt-Marie M. Anderlid, Jacqueline Schoumans, Nine V. Knoers, Ad Geurts G. van Kessel, Erik A. Sistermans, Joris A. Veltman, Han G. Brunner, Bert B. de Vries posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:56:36 as
	Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. [My Copy] Nature genetics, Vol. 38, No. 9. (13 September 2006), pp. 1038-1042. by Andrew J. Sharp, Sierra Hansen, Rebecca R. Selzer, et al.Ze Cheng, Regina Regan, Jane A. Hurst, Helen Stewart, Sue M. Price, Edward Blair, Raoul C. Hennekam, Carrie A. Fitzpatrick, Rick Segraves, Todd A. Richmond, Cheryl Guiver, Donna G. Albertson, Daniel Pinkel, Peggy S. Eis, Stuart Schwartz, Samantha J. Knight, Evan E. Eichler posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:53:42 as along with 1 person waszak
	Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2. [My Copy] Nature genetics, Vol. 39, No. 9. (19 September 2007), pp. 1071-1073. by Blake C. Ballif, Sara A. Hornor, Elizabeth Jenkins, et al.Suneeta Madan-Khetarpal, Urvashi Surti, Kelly E. Jackson, Alexander Asamoah, Pamela L. Brock, Gordon C. Gowans, Robert L. Conway, John M. Graham, Livija Medne, Elaine H. Zackai, Tamim H. Shaikh, Joel Geoghegan, Rebecca R. Selzer, Peggy S. Eis, Bassem A. Bejjani, Lisa G. Shaffer posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:37:01 as
	De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy. [My Copy] Annals of neurology, Vol. 65, No. 6. (June 2009), pp. 748-753. by Fadi F. Hamdan, Amélie Piton, Julie Gauthier, et al.Anne Lortie, François Dubeau, Sylvia Dobrzeniecka, Dan Spiegelman, Anne Noreau, Stéphanie Pellerin, Mélanie Côté, Edouard Henrion, Eric Fombonne, Laurent Mottron, Claude Marineau, Pierre Drapeau, Ronald G. Lafrenière, Jean Claude C. Lacaille, Guy A. Rouleau, Jacques L. Michaud posted to synaptic neurogen mr humgen epilep brainmut by daforerog on 2009-09-14 15:58:39 as
	Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation. [My Copy] The New England journal of medicine, Vol. 360, No. 6. (5 February 2009), pp. 599-605. by Fadi F. Hamdan, Julie Gauthier, Dan Spiegelman, et al.Anne Noreau, Yan Yang, Stéphanie Pellerin, Sylvia Dobrzeniecka, Mélanie Côté, Elizabeth Perreault-Linck, Lionel Carmant, Guy D'Anjou, Eric Fombonne, Anjene M. Addington, Judith L. Rapoport, Lynn E. Delisi, Marie-Odile O. Krebs, Faycal Mouaffak, Ridha Joober, Laurent Mottron, Pierre Drapeau, Claude Marineau, Ronald G. Lafrenière, Jean Claude C. Lacaille, Guy A. Rouleau, Jacques L. Michaud, Synapse to Disease Group posted to synaptic nssnps mr humgen brainmut by daforerog on 2009-09-14 15:38:31 as
	Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. [My Copy] Journal of medical genetics, Vol. 46, No. 8. (21 August 2009), pp. 511-523. by B. W. van Bon, H. C. Mefford, B. Menten, et al.D. A. Koolen, A. J. Sharp, W. M. Nillesen, J. W. Innis, T. J. de Ravel, C. L. Mercer, M. Fichera, H. Stewart, L. E. Connell, K. Ounap, K. Lachlan, B. Castle, N. Van der Aa, C. van Ravenswaaij, M. A. Nobrega, C. Serra-Juhé, I. Simonic, N. de Leeuw, R. Pfundt, E. M. Bongers, C. Baker, P. Finnemore, S. Huang, V. K. Maloney, J. A. Crolla, M. van Kalmthout, M. Elia, G. Vandeweyer, J. P. Fryns, S. Janssens, N. Foulds, S. Reitano, K. Smith, S. Parkel, B. Loeys, C. G. Woods, A. Oostra, F. Speleman, A. C. Pereira, A. Kurg, L. Willatt, S. J. Knight, J. R. Vermeesch, C. Romano, J. C. Barber, G. Mortier, L. A. Pérez-Jurado, F. Kooy, H. G. Brunner, E. E. Eichler, T. Kleefstra, B. B. de Vries posted to neurogen mr humgen cnv by daforerog on 2009-09-14 14:01:28 as along with 1 person bmenten
	A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. [My Copy] Nature genetics, Vol. 40, No. 3. (17 March 2008), pp. 322-328. by Andrew J. Sharp, Heather C. Mefford, Kelly Li, et al.Carl Baker, Cindy Skinner, Roger E. Stevenson, Richard J. Schroer, Francesca Novara, Manuela De Gregori, Roberto Ciccone, Adam Broomer, Iris Casuga, Yu Wang, Chunlin Xiao, Catalin Barbacioru, Giorgio Gimelli, Bernardo Dalla D. Bernardina, Claudia Torniero, Roberto Giorda, Regina Regan, Victoria Murday, Sahar Mansour, Marco Fichera, Lucia Castiglia, Pinella Failla, Mario Ventura, Zhaoshi Jiang, Gregory M. Cooper, Samantha J. Knight, Corrado Romano, Orsetta Zuffardi, Caifu Chen, Charles E. Schwartz, Evan E. Eichler posted to neuropsygen neurogen mr humgen epilep cnv by daforerog on 2009-09-14 13:57:07 as
	Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. [My Copy] The New England journal of medicine, Vol. 359, No. 16. (16 October 2008), pp. 1685-1699. by Heather C. Mefford, Andrew J. Sharp, Carl Baker, et al.Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv K. Maloney, John A. Crolla, Diana Baralle, Amanda Collins, Catherine Mercer, Koen Norga, Thomy de Ravel, Koen Devriendt, Ernie M. Bongers, Nicole de Leeuw, William Reardon, Stefania Gimelli, Frederique Bena, Raoul C. Hennekam, Alison Male, Lorraine Gaunt, Jill Clayton-Smith, Ingrid Simonic, Soo Mi M. Park, Sarju G. Mehta, Serena Nik-Zainal, C. Geoffrey Woods, Helen V. Firth, Georgina Parkin, Marco Fichera, Santina Reitano, Mariangela Lo Giudice, Kelly E. Li, Iris Casuga, Adam Broomer, Bernard Conrad, Markus Schwerzmann, Lorenz Räber, Sabina Gallati, Pasquale Striano, Antonietta Coppola, John L. Tolmie, Edward S. Tobias, Chris Lilley, Lluis Armengol, Yves Spysschaert, Patrick Verloo, Anja De Coene, Linde Goossens, Geert Mortier, Frank Speleman, Ellen van Binsbergen, Marcel R. Nelen, Ron Hochstenbach, Martin Poot, Louise Gallagher, Michael Gill, Jon McClellan, Mary-Claire C. King, Regina Regan, Cindy Skinner, Roger E. Stevenson, Stylianos E. Antonarakis, Caifu Chen, Xavier Estivill, Björn Menten, Giorgio Gimelli, Susan Gribble, Stuart Schwartz, James S. Sutcliffe, Tom Walsh, Samantha J. Knight, Jonathan Sebat, Corrado Romano, Charles E. Schwartz, Joris A. Veltman, Bert B. de Vries, Joris R. Vermeesch, John C. Barber, Lionel Willatt, May Tassabehji, Evan E. Eichler posted to psychgen mr humgen cnv assoc by daforerog on 2009-09-08 15:44:17 as along with 2 people jbhiatt bmenten
	Neuroradiological features of vertigo. [My Copy] Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, Vol. 25 Suppl 1 (March 2004) by M. G. Bruzzone, M. Grisoli, T. De Simone, C. Regna-Gladin posted to vertigo mr by thenose on 2009-09-08 04:26:32 as
	Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex. [My Copy] European journal of human genetics : EJHG, Vol. aop, No. current. (22 July 2009) by Martin Poot, Marc J. Eleveld, Ruben van 't Slot, Hans Kristian K. Ploos van Amstel, Ron Hochstenbach posted to synaptic mr humgen genomics cnv assoc by daforerog on 2009-08-27 13:42:42 as
	Abnormal Signal Intensity in Skeletal Muscle at MR Imaging: Patterns, Pearls, and Pitfalls1 [My Copy] Radiographics, Vol. 20, No. suppl 1. (October 2000), pp. S295-S315. by David A. May, David G. Disler, Elizabeth A. Jones, Avinash A. Balkissoon, B. J. Manaster posted to myositis mr bone by kapur on 2009-08-18 18:27:46 as
	Advances of 3T MR imaging in visualizing trabecular bone structure of the calcaneus are partially SNR-independent: Analysis using simulated noise in relation to micro-CT, 1.5T MRI, and biomechanical strength [My Copy] Journal of Magnetic Resonance Imaging, Vol. 29, No. 1. (2009), pp. 132-140. by Jan S. Bauer, Roberto Monetti, Roland Krug, et al.Maiko Matsuura, Dirk Mueller, Felix Eckstein, Ernst J. Rummeny, Eva-Maria Lochmueller, Christoph W. Raeth, Thomas M. Link posted to ct mr osteoporosis by mdifranc on 2009-07-30 12:25:16 as
	The role of neuronal complexes in human X-linked brain diseases. [My Copy] American journal of human genetics, Vol. 80, No. 2. (February 2007), pp. 205-220. by F. Laumonnier, P. C. Cuthbert, S. G. Grant posted to assoc highly humgen mining mr neuropsygen synaptic systems by daforerog on 2009-07-28 15:20:30 as
	Genes, plasticity and mental retardation. [My Copy] Behavioural brain research, Vol. 192, No. 1. (1 September 2008), pp. 88-105. by C. Vaillend, R. Poirier, S. Laroche posted to brain mr review synaptic by daforerog on 2009-07-24 15:43:43 as
	X-linked mental retardation: focus on synaptic function and plasticity. [My Copy] Journal of neurochemistry, Vol. 109, No. 1. (April 2009), pp. 1-14. by Y. Humeau, F. Gambino, J. Chelly, N. Vitale posted to mr neurogen review synaptic by daforerog on 2009-07-24 15:28:06 as
	X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment. [My Copy] Nature genetics, Vol. 40, No. 6. (11 June 2008), pp. 776-781. by L. M. Dibbens, P. S. Tarpey, K. Hynes, et al.M. A. Bayly, I. E. Scheffer, R. Smith, J. Bomar, E. Sutton, L. Vandeleur, C. Shoubridge, S. Edkins, S. J. Turner, C. Stevens, S. O'Meara, C. Tofts, S. Barthorpe, G. Buck, J. Cole, K. Halliday, D. Jones, R. Lee, M. Madison, T. Mironenko, J. Varian, S. West, S. Widaa, P. Wray, J. Teague, E. Dicks, A. Butler, A. Menzies, A. Jenkinson, R. Shepherd, J. F. Gusella, Z. Afawi, A. Mazarib, M. Y. Neufeld, S. Kivity, D. Lev, T. Lerman-Sagie, A. D. Korczyn, C. P. Derry, G. R. Sutherland, K. Friend, M. Shaw, M. Corbett, H. G. Kim, D. H. Geschwind, P. Thomas, E. Haan, S. Ryan, S. McKee, S. F. Berkovic, P. A. Futreal, M. R. Stratton, J. C. Mulley, J. Gécz posted to brainmut epilep humgen mr nssnps synaptic by daforerog on 2009-07-15 15:56:29 as
	Fast and robust registration of PET and MR images of human brain. [My Copy] NeuroImage, Vol. 22, No. 1. (May 2004), pp. 434-442. by J. Cízek, K. Herholz, S. Vollmar, R. Schrader, J. Klein, W. D. Heiss posted to and brain fast human images mr of pet registration robust by djahny on 2009-07-08 04:00:10 as
	Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease. [My Copy] American journal of human genetics, Vol. 76, No. 4. (April 2005), pp. 572-580. by J. H. Roelfsema, S. J. White, Y. Ariyürek, et al.D. Bartholdi, D. Niedrist, F. Papadia, C. A. Bacino, J. T. den Dunnen, G. J. van Ommen, M. H. Breuning, R. C. Hennekam, D. J. Peters posted to brainmut humgen mr synaptic by daforerog on 2009-07-06 15:17:45 as
	Diffusion-weighted MR imaging of acute stroke: correlation with T2-weighted and magnetic susceptibility-enhanced MR imaging in cats. [My Copy] AJNR. American journal of neuroradiology, Vol. 11, No. 3. (May 1990), pp. 423-429. by M. E. Moseley, J. Kucharczyk, J. Mintorovitch, et al.Y. Cohen, J. Kurhanewicz, N. Derugin, H. Asgari, D. Norman posted to diffusion-weighted moseley_me mr by Explorer on 2009-06-30 20:43:24 as
	What is the current role of CT urography and MR urography in the evaluation of the urinary tract? [My Copy] Radiology, Vol. 250, No. 2. (1 February 2009), pp. 309-323. by S. G. Silverman, J. R. Leyendecker, E. S. Amis posted to mr uro mruro by throstur on 2009-06-30 17:41:50 as along with 1 person and 1 group dr_lee_xray MEHTRadiology
	Contrast medium issues in MR urography. [My Copy] Academic radiology, Vol. 16, No. 6. (June 2009), pp. 772-772. by P. H. Vivier, J. N. Dacher posted to mr uro mruro by throstur on 2009-06-30 16:25:34 as
	A functional form for injected MRI Gd-chelate contrast agent concentration incorporating recirculation, extravasation and excretion [My Copy] Physics in Medicine and Biology, Vol. 54, No. 9. (2009), pp. 2933-2949. by Mark A. Horsfield, John S. Thornton, Andrew Gill, Rolf H. Jager, Andrew N. Priest, Bruno Morgan posted to aif dce dual-input liver mr by anitabanerji on 2009-06-26 14:47:01 as
	CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait [My Copy] PLoS Genet, Vol. 5, No. 5. (22 May 2009), e1000487. by Seval Türkmen, Gao Guo, Masoud Garshasbi, et al.Katrin Hoffmann, Amjad J. Alshalah, Claudia Mischung, Andreas Kuss, Nicholas Humphrey, Stefan Mundlos, Peter N. Robinson posted to brainmut humgen mr neurogen nssnps by daforerog on 2009-06-25 11:28:25 as along with 2 people darian Schmidtc
	Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, No. 46. (13 November 2007), pp. 18163-18168. by Y. Wu, A. C. Arai, G. Rumbaugh, et al.A. K. Srivastava, G. Turner, T. Hayashi, E. Suzuki, Y. Jiang, L. Zhang, J. Rodriguez, J. Boyle, P. Tarpey, F. L. Raymond, J. Nevelsteen, G. Froyen, M. Stratton, A. Futreal, J. Gecz, R. Stevenson, C. E. Schwartz, D. Valle, R. L. Huganir, T. Wang posted to assoc brainmut humgen mr synaptic systems by daforerog on 2009-06-24 11:53:46 as
	An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertion [My Copy] European Journal of Human Genetics, Vol. aop, No. current. by Helle Lyb￦k, Karen H. Ørstavik, Trine Prescott, et al.Randi Hovland, Harald Breilid, Christine Stansberg, Vidar M. Steen, Gunnar Houge posted to assoc cnv humgen mr synaptic by daforerog on 2009-06-23 12:25:23 as
	Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome. [My Copy] American journal of human genetics, Vol. 84, No. 6. (June 2009), pp. 728-739. by J. Armistead, S. Khatkar, B. Meyer, et al.B. L. Mark, N. Patel, G. Coghlan, R. E. Lamont, S. Liu, J. Wiechert, P. A. Cattini, P. Koetter, K. Wrogemann, C. R. Greenberg, K. D. Entian, T. Zelinski, B. Triggs-Raine posted to brainmut humgen mr neurogen by daforerog on 2009-06-19 14:59:50 as
	Interpretation of Intelligence Test Scores in <i>Atkins</i> Cases: Conceptual and Psychometric Issues [My Copy] Applied Neuropsychology, Vol. 16, No. 2. (2009), pp. 91-97. by Frank M. Gresham posted to intelligence measurement_error mr by jjdemann on 2009-06-16 18:43:01 as
	Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders. [My Copy] Journal of medical genetics, Vol. 46, No. 6. (June 2009), pp. 382-388. by S. Ben-Shachar, B. Lanpher, J. R. German, et al.M. Qasaymeh, L. Potocki, S. C. Nagamani, L. M. Franco, A. Malphrus, G. W. Bottenfield, J. E. Spence, S. Amato, J. A. Rousseau, B. Moghaddam, C. Skinner, S. A. Skinner, S. Bernes, N. Armstrong, M. Shinawi, P. Stankiewicz, A. Patel, S. W. Cheung, J. R. Lupski, A. L. Beaudet, T. Sahoo posted to autism cnv mr psychgen by daforerog on 2009-06-15 21:50:34 as
	MR imaging of lumbar facet joint synovial cysts [My Copy] European Radiology, Vol. 10, No. 4. (15 March 2000), pp. 615-623. by E. Apostolaki, A. M. Davies, N. Evans, V. N. Cassar-Pullicino posted to cysts facet joint mr synovial by dr_lee_xray to the group MEHTRadiology on 2009-06-04 19:32:31 as
	Automatic Segmentation of the Caudate Nucleus From Human Brain MR Images [My Copy] Medical Imaging, IEEE Transactions on In Medical Imaging, IEEE Transactions on, Vol. 26, No. 4. (2007), pp. 509-517. by Yan Xia, K. Bettinger, Lin Shen, A. L. Reiss posted to brain caudate mr nucleus segmentation by carlding on 2009-06-01 07:57:47 as
	Classification of Dynamic Contrast-Enhanced Magnetic Resonance Breast Lesions by Support Vector Machines [My Copy] Medical Imaging, IEEE Transactions on In Medical Imaging, IEEE Transactions on, Vol. 27, No. 5. (2008), pp. 688-696. by J. Levman, T. Leung, P. Causer, D. Plewes, A. L. Martel posted to classification mr svm by carlding on 2009-06-01 07:18:51 as along with 1 person xtizon
	Mitral regurgitation [My Copy] The Lancet, Vol. 373, No. 9672. (24 April 2009), pp. 1382-1394. by Maurice Enriquez-Sarano, Cary W. Akins, Alec Vahanian posted to mr by guhjy on 2009-05-27 05:42:51 as
	XLMR genes: update 2007 [My Copy] European Journal of Human Genetics, Vol. aop, No. current. by Pietro Chiurazzi, Charles E. Schwartz, Jozef Gecz, Giovanni Neri posted to assoc brainmut humgen mining mr neurogen neuropsygen psychgen by daforerog on 2009-05-21 23:05:06 as along with 1 person dchughes
	Assessing local residence time distributions in screw extruders through a new in-line measurement instrument [My Copy] Polymer Engineering & Science, Vol. 46, No. 4. (2006), pp. 510-519. by Xian-Ming Zhang, Zhong-Bin Xu, Lian-Fang Feng, Xiao-Bo Song, Guo-Hua Hu posted to mr by 6rheology on 2009-05-19 05:41:57 as

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