Zobrazeno 1 - 2
of 2
pro vyhledávání: '"X J de Mollerat"'
Autor:
R Fischetto, Fiorella Gurrieri, Charles E. Schwartz, F Causio, Eugenio Sangiorgi, X J de Mollerat, D Tackels-Horne, A Toburen, Katie Clarkson, Roger E. Stevenson
Publikováno v:
Clinical Genetics. 59:28-36
Developmental anomalies of the appendicular skeleton are among the most common and easily ascertained birth defects. Split hand/split foot malformations, distinctive in having deficiency of the central rays, occur as isolated anomalies and as one com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::099baf3ada0b5d76460155bc2a0ddfa3
https://doi.org/10.1034/j.1399-0004.2001.590105.x
https://doi.org/10.1034/j.1399-0004.2001.590105.x
Autor:
Arthur S. Aylsworth, David B. Everman, Chad T. Morgan, R. C. Rogers, John M. Graham, Charles E. Schwartz, R S Colby, X J de Mollerat, Katie Clarkson, Roger E. Stevenson
Publikováno v:
Journal of medical genetics. 40(1)
Ectrodactyly or split hand/foot malformation (SHFM) is a human limb malformation characterised by underdevelopment or absence of the central digital rays and variable fusion of the remaining digits (MIM 183600). This condition occurs in 1 in 8500–2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::390fc1a1d92e4e15b8acd1ccd2e5d88f
https://pubmed.ncbi.nlm.nih.gov/12525544
https://pubmed.ncbi.nlm.nih.gov/12525544