Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Cason, A. Lauren"'
Autor:
MacMillan Andrée, Macgregor David, Holinski-Feder Elke, Mangelsdorf Marie, Finnis Merran, Cason A Lauren, Stepp Monica L, Holden Jeanette JA, Gecz Jozef, Stevenson Roger E, Schwartz Charles E
Publikováno v:
BMC Medical Genetics, Vol 6, Iss 1, p 16 (2005)
Abstract Background X-linked mental retardation (XLMR) is the leading cause of mental retardation in males. Mutations in the ARX gene in Xp22.1 have been found in numerous families with both nonsyndromic and syndromic XLMR. The most frequent mutation
Externí odkaz:
https://doaj.org/article/338cd399448d4c11b86065723c7421b5
Autor:
Stepp, Monica L1 mdlindsey@ggc.org, Cason, A Lauren1 cason@musc.edu, Finnis, Merran2 merranfinnis@yahoo.com, Mangelsdorf, Marie2,3 mmangelsdorf@ohri.ca, Holinski-Feder, Elke4 Holinski-Feder@mgz-muenchen.de, Macgregor, David5 david.macgregor@hccsj.nl.ca, MacMillan, Andree6 Andree.MacMillan@hccsj.nf.ca, Holden, Jeanette JA7 holdenj@post.QueensU.CA, Gecz, Jozef2,3 jozef.gecz@adelaide.edu.au, Stevenson, Roger E1 res@ggc.org, Schwartz, Charles E1 ceschwartz@ggc.org
Publikováno v:
BMC Medical Genetics. 2005, Vol. 6, p16-4. 4p. 1 Graph.
Autor:
Cason, A. Lauren1, Ikeguchi, Yoshihiko2, Skinner, Cindy1, Wood, Tim C.1, Holden, Kenton R.1, Lubs, Herbert A.3, Martinez, Francisco4, Simensen, Richard J.1, Stevenson, Roger E.1, Pegg, Anthony E.2, Schwartz, Charles E.1 schwartz@ggc.org
Publikováno v:
European Journal of Human Genetics. Dec2003, Vol. 11 Issue 12, p937-944. 8p.