Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.
(Q41145529)
scientific article published on October 1995
scientific article published on October 1995
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Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.
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description | scientific article published on October 1995 |
External Links
(P356) |
10.1002/AJMG.1320590122
|
(P698) |
8849001
|