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Article

Adams-Oliver syndrome, a family with dominant inheritance and a severe phenotype.

Clinical dysmorphology - 1 Oct 2011

Vandersteen Anthony M, Dixon Joanne W

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 21785343
DOI: 10.1097/MCD.0b013e32834964d1

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DLL4 loss-of-function heterozygous mutations cause Adams-Oliver syndrome.Semantic proximity Read ↗

Characterization of a New Variant in ARHGAP31 Probably Involved in Adams-Oliver Syndrome in a Family with a Variable Phenotypic Spectrum.Semantic proximity Read ↗

Polymicrogyria associated with scalp and limb defects: Variant of Adams-Oliver syndromeSemantic proximity Read ↗

Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort.Semantic proximity Read ↗

Adams-Oliver syndrome: autosomal recessive inheritance and new phenotypic-anthropometric findings.Semantic proximity Read ↗

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Mutations in NOTCH1 cause Adams-Oliver syndrome.Semantic proximity Read ↗

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