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Mutations in the CHX10 gene in non‐syndromic microphthalmia/anophthalmia patients from Qatar
Author(s) -
FaiyazUlHaque M,
Zaidi SHE,
AlMureikhi MS,
Peltekova I,
Tsui LC,
Teebi AS
Publication year - 2007
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.1399-0004.2007.00846.x
Subject(s) - medical genetics , sick child , medicine , family medicine , genetics , pediatrics , biology , gene
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