Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2 (Q28284655)
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Current Data About Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2
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(P1932) J M Opitz

(P304) 459-61

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(P577) +1995-12-00T00:00:00Z

(P1433) (Q976454)

(P1476) "Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2" (language: en)

(P2093) N H Robin
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G J Feldman
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A L Aronson
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H F Mitchell
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R Weksberg
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C O Leonard
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B K Burton
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K D Josephson
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R Laxová
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K A Aleck
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J E Allanson
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M L Guion-Almeida
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R A Martin
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L G Leichtman
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R A Price
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M Muenke
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(P854) https://api.crossref.org/works/10.1038%2FNG1295-459
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(P854) https://api.crossref.org/works/10.1038%2FNG1295-459
(P813) Thursday, January 7, 2021
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(P854) https://api.crossref.org/works/10.1038%2FNG1295-459
(P813) Thursday, January 7, 2021
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(Q27860521)
(P248)
(P854) https://api.crossref.org/works/10.1038%2FNG1295-459
(P813) Thursday, January 7, 2021
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External Links
(P356) 10.1038/NG1295-459
(P698) 7493033
(P3181) 2283114
(P5875) 15706134