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A new STAR on the horizon
Author(s) -
Visscher H
Publication year - 2008
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2008.01065_2.x
Subject(s) - syndactyly , genetics , biology , mutation , medicine , gene
Mutations in the cyclin family member FAM58A cause an X‐linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations
Unger et al. (2008)
Nature Genetics 40: 287–289