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Autosomal dominant “Opitz” GBBB syndrome due to a 22q11. 2 deletion |
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| Authors: | Donna M. McDonald-McGinn Deborah A. Driscoll Lynn Bason Katherine Christensen David Lynch Kathleen Sullivan Douglas Canning William Zavod Norman Quinn Jonathan Rome Yvonne Paris Paul Weinberg Bernard J. Clark Beverly S. Emanuel Elaine H. Zackai |
| Abstract: | |
| Keywords: | Opitz GBBB syndrome BBB syndrome G syndrome hypertelorism-hypospadias 22q11.2 deletion DiGeorge syndrome velocardiofacial syndrome CTAF (conotruncal anomaly face syndrome) |