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American Journal of Human Genetics|February 11, 1999
DNA rearrangements on both homologues of chromosome 17 in a mildly delayed individual with a family history of autosomal dominant carpal tunnel syndromeL Potocki, K S Chen, T Koeuth, et al.Human Genetics|May 1, 1996
Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathyB B Roa, F Greenberg, P Gunaratne, et al.Clinical Immunology (Orlando, Fla.)|May 31, 2008
Monosomy 1p36 uncovers a role for OX40 in survival of activated CD4+ T cellsM M Suhoski, E E Perez, M L Heltzer, et al.American Journal of Human Genetics|April 1, 1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11O Bartsch, W Wuyts, W Van Hul, et al.Genomics|August 17, 2000
Isolation and preliminary characterization of the human and mouse homologues of the bacterial cell cycle gene eraR A Britton, S M Chen, D Wallis, et al.American Journal of Medical Genetics|December 18, 1998
Inherited duplication Xq27-qter at Xp22.3 in severely affected males: molecular cytogenetic evaluation and clinical description in three unrelated familiesB K Goodman, L G Shaffer, J Rutberg, et al.Epilepsia|October 3, 2001
Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndromeH A Heilstedt, D L Burgess, A E Anderson, et al.Nature Genetics|December 30, 1999
Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletionL Potocki, K S Chen, S S Park, et al.Human Genetics|January 24, 1998
Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalitiesE Schröck, T Veldman, H Padilla-Nash, et al.Molecular Syndromology|November 1, 2012
Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 MicrodeletionsR N Traylor, W B Dobyns, J A Rosenfeld, et al.Pageof 22