These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
77 related articles for article (PubMed ID: 7676123)
21. Identification of a mutant allele of the androgen receptor gene in a family with androgen insensitivity syndrome: detection of carriers and prenatal diagnosis. Fogu G; Bertini V; Dessole S; Bandiera P; Campus PM; Capobianco G; Sanna R; Soro G; Montella A Arch Gynecol Obstet; 2004 May; 269(4):266-9. PubMed ID: 12898143 [TBL] [Abstract][Full Text] [Related]
22. Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24. van der Vleuten AJ; van Ravenswaaij-Arts CM; Frijns CJ; Smits AP; Hageman G; Padberg GW; Kremer H Eur J Hum Genet; 1998; 6(4):376-82. PubMed ID: 9781046 [TBL] [Abstract][Full Text] [Related]
23. CAG repeat contraction in the androgen receptor gene in three brothers with mental retardation. Kooy RF; Reyniers E; Storm K; Vits L; van Velzen D; de Ruiter PE; Brinkmann AO; de Paepe A; Willems PJ Am J Med Genet; 1999 Jul; 85(3):209-13. PubMed ID: 10398229 [TBL] [Abstract][Full Text] [Related]
25. Larger trinucleotide repeat size in the androgen receptor gene of infertile men with extremely severe oligozoospermia. Patrizio P; Leonard DG; Chen KL; Hernandez-Ayup S; Trounson AO J Androl; 2001; 22(3):444-8. PubMed ID: 11330644 [TBL] [Abstract][Full Text] [Related]
26. Missense mutation in exon 7 of the common gamma chain gene causes a moderate form of X-linked combined immunodeficiency. Schmalstieg FC; Leonard WJ; Noguchi M; Berg M; Rudloff HE; Denney RM; Dave SK; Brooks EG; Goldman AS J Clin Invest; 1995 Mar; 95(3):1169-73. PubMed ID: 7883965 [TBL] [Abstract][Full Text] [Related]
27. [A case of Kennedy-Alter-Sung (KAS) syndrome presenting as hypersexuality and elevated serum CK: usefulness of genetic analysis]. Hokezu Y; Yanai S; Nagai M; Nagamatsu K; Yamamoto Y Rinsho Shinkeigaku; 1996 Mar; 36(3):471-4. PubMed ID: 8741352 [TBL] [Abstract][Full Text] [Related]
28. [A weak man... X chromosome associated progressive bulbospinal neuropathy (or bulbospinal amyotrophy) or Kennedy syndrome]. Ricard D; Sallansonnet-Froment M; De Greslan T Rev Neurol (Paris); 2009 Feb; 165 Spec No 1():F29, F31. PubMed ID: 19623708 [No Abstract] [Full Text] [Related]
29. Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome. Hertz JM; Juncker I; Persson U; Matthijs G; Schmidtke J; Petersen MB; Kjeldsen M; Gregersen N Hum Mutat; 2001 Aug; 18(2):141-8. PubMed ID: 11462238 [TBL] [Abstract][Full Text] [Related]
30. [The DNA diagnosis of a familial case of Kennedy's spinal and bulbar amyotrophy]. Petrukhin AS; Zavadenko NN; Petrukhin AA; Evgrafov OV Zh Nevrol Psikhiatr Im S S Korsakova; 1997; 97(3):45-8. PubMed ID: 9157759 [TBL] [Abstract][Full Text] [Related]
31. Inheritance of skewed X chromosome inactivation in a large family with an X-linked recessive deafness syndrome. Orstavik KH; Orstavik RE; Eiklid K; Tranebjaerg L Am J Med Genet; 1996 Jul; 64(1):31-4. PubMed ID: 8826445 [TBL] [Abstract][Full Text] [Related]
32. X-linked recessive bulbospinal neuronopathy (SBMA). Sobue G Nagoya J Med Sci; 1995 Dec; 58(3-4):95-106. PubMed ID: 8725492 [TBL] [Abstract][Full Text] [Related]