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Primary skeletal dysplasia as a major manifesting feature in an infant with congenital disorder of glycosylation type Ia
Author(s) -
Coman D.,
Bostock D.,
Hunter M.,
Kannu P.,
Irving M.,
Mayne V.,
Fietz M.,
Jaeken J.,
Savarirayan R.
Publication year - 2008
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.32119
Subject(s) - medicine , referral , family medicine , library science , pediatrics , gerontology , computer science