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Showing results (661-670 of 719) with videos related to

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Human Molecular Genetics|July 3, 2003
Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerveStefano C Previtali, Barbara Zerega, Diane L Sherman, et al.
Genomics|November 5, 1997
A sequence-ready physical map of a region of 12q24.1B Renault, A Hovnanian, S Bryce, et al.
Archives of Neurology|November 14, 2007
Choreoacanthocytosis in a Mexican familyJosé L Ruiz-Sandoval, Víctor García-Navarro, Erwin Chiquete, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
A 15q13.3 microdeletion segregating with autismAlistair T Pagnamenta, Kirsty Wing, Elham Sadighi Akha, et al.
Genomics|October 27, 1997
Novel genes mapping to the critical region of the 5q- syndromeJ Boultwood, C Fidler, P Soularue, et al.
American Journal of Human Genetics|April 11, 2003
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11Matthew N Ogdie, I Laurence Macphie, Sonia L Minassian, et al.
Journal of Neurodevelopmental Disorders|June 17, 2016
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypesKerry A Pettigrew, Emily Frinton, Ron Nudel, et al.
Nature Genetics|May 10, 2000
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2A Bolino, M Muglia, F L Conforti, et al.
Genomics|September 24, 1999
Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3)A H Németh, D Nolte, E Dunne, et al.
Human Molecular Genetics|April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pumpR Sudbrak, J Brown, C Dobson-Stone, et al.
Pageof 72

Showing results (661-670 of 719) with videos related to

Sort By:
Pageof 72
Human Molecular Genetics|July 3, 2003
Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerveStefano C Previtali, Barbara Zerega, Diane L Sherman, et al.
Genomics|November 5, 1997
A sequence-ready physical map of a region of 12q24.1B Renault, A Hovnanian, S Bryce, et al.
Archives of Neurology|November 14, 2007
Choreoacanthocytosis in a Mexican familyJosé L Ruiz-Sandoval, Víctor García-Navarro, Erwin Chiquete, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
A 15q13.3 microdeletion segregating with autismAlistair T Pagnamenta, Kirsty Wing, Elham Sadighi Akha, et al.
Genomics|October 27, 1997
Novel genes mapping to the critical region of the 5q- syndromeJ Boultwood, C Fidler, P Soularue, et al.
American Journal of Human Genetics|April 11, 2003
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11Matthew N Ogdie, I Laurence Macphie, Sonia L Minassian, et al.
Journal of Neurodevelopmental Disorders|June 17, 2016
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypesKerry A Pettigrew, Emily Frinton, Ron Nudel, et al.
Nature Genetics|May 10, 2000
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2A Bolino, M Muglia, F L Conforti, et al.
Genomics|September 24, 1999
Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3)A H Németh, D Nolte, E Dunne, et al.
Human Molecular Genetics|April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pumpR Sudbrak, J Brown, C Dobson-Stone, et al.
Pageof 72