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Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

✍ Scribed by Robin, Nathaniel H.; Feldman, George J.; Aronson, Adam L.; Mitchell, Heather F.; Weksberg, Rosanna; Leonard, Claire O.; Burton, Barbara K.; Josephson, Kevin D.; Laxová, Renata; Aleck, Kyrieckos A.

Book ID: 109918898
Publisher: Nature Publishing Group
Year: 1995
Tongue: English
Weight: 320 KB
Volume: 11
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng1295-459

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