Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2 (Q28284655)

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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

https://scigraph.springernature.com/pub.10.1038/ng1295-459

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language of work or name

English

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publication date

December 1995

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published in

Nature Genetics

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volume

11

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issue

4

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page(s)

459-61

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exact match

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cites work

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G syndrome (hypertelorism with esophageal abnormality and hypospadias, or hypospadias-dysphagia, or "Opitz-Frias" or "Opitz-G" syndrome)--perspective in 1987 and bibliography

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Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

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Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

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Cloning of six new genes with zinc finger motifs mapping to short and long arms of human acrocentric chromosome 22 (p and q11.2)

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