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Human Genetics|February 1, 1991
Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosisB A van Oost, P M van Zandvoort, W Tünte, et al.Journal of Medical Genetics|October 23, 1998
Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26H G Yntema, B C Hamel, A P Smits, et al.American Journal of Human Genetics|August 1, 1990
Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell linesG K Suthers, V J Hyland, D F Callen, et al.Genomics|September 7, 2001
Genomic organization and expression of the doublesex-related gene cluster in vertebrates and detection of putative regulatory regions for DMRT1B Brunner, U Hornung, Z Shan, et al.Journal of Medical Genetics|August 21, 2008
High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart diseaseF Erdogan, L A Larsen, L Zhang, et al.Science (New York, N.Y.)|February 3, 1995
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.Human Genetics|October 1, 1993
Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpointsR J Sinke, B de Leeuw, H A Janssen, et al.American Journal of Human Genetics|May 1, 1995
The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter regionM Wijker, M J Ligtenberg, F Schoute, et al.Annals of Neurology|October 1, 1994
Prevalence of the 1.5-Mb 17p deletion in families with hereditary neuropathy with liability to pressure palsiesE C Mariman, A A Gabreëls-Festen, S E van Beersum, et al.Journal of Medical Genetics|June 28, 2005
Breakpoints around the HOXD cluster result in various limb malformationsB Dlugaszewska, A Silahtaroglu, C Menzel, et al.Pageof 21