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Article

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

1 Dec 1995

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7493033
DOI: 10.1038/ng1295-459

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2PMID 7493033Read ↗

A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients.Semantic proximity Read ↗

Holt–Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12qSemantic proximity Read ↗

Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndromeSemantic proximity Read ↗

Smith-Lemli-Opitz syndrome: further delineation of the phenotype.Semantic proximity Read ↗

The 22q11.2 Deletion SyndromeSemantic proximity Read ↗

De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome.Semantic proximity Read ↗

A microdeletion 22q11.2 can resemble Shprintzen-Goldberg omphalocele syndrome.Semantic proximity Read ↗

Monozygotic twins with 22q11 deletion and discordant phenotypes.Semantic proximity Read ↗

Multidisciplinary management of Opitz G BBB syndrome.Semantic proximity Read ↗

22q11.2 deletion syndromeSemantic proximity Read ↗

Opitz G/BBB syndrome: Clinical comparisons of families linked to Xp22 and 22Q and a review of the literatureSemantic proximity Read ↗

Hypospadias associated with hypertelorism, the mildest phenotype of Opitz syndrome.Semantic proximity Read ↗

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