Výsledky vyhledávání - "S. H.E. Zaidi"

A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13

Autor: LC Tsui, S Meyer, S. H.E. Zaidi, A D Paterson, A Lindinger, Ahmad S. Teebi, VD Peltekova, Muhammad Faiyaz-Ul-Haque

Publikováno v: Clinical Genetics. 67:183-188

Arterial tortuosity associated with hyperextensible skin and hypermobility of joints, features that are characteristics of Ehlers-Danlos syndrome (EDS), has been described in several families. An arterial tortuosity locus has recently been mapped to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5b111cba2fe0b4af65e31debd4e53025
https://doi.org/10.1111/j.1399-0004.2004.00391.x

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Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes

Autor: Muhammad Faiyaz-Ul-Haque, Wasim Ahmad, Lily King, Daniel H. Cohn, M. Patel, Teepu Siddique, LC Tsui, Sayedul Haque, Mahmud Ahmad, S. H.E. Zaidi

Publikováno v: Clinical Genetics. 67:93-97

Split-hand/split-foot malformation (SHFM) is a genetically heterogeneous disorder, with five known loci, that causes a lack of median digital rays, syndactyly, and aplasia or hypoplasia of the phalanges, metacarpals, and metatarsals. In the only know

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c68dc5c1ffcacce80e52d7de07971f9e
https://doi.org/10.1111/j.1399-0004.2004.00369.x

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