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Article

Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly

18 Jan 2012

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22258522
DOI: 10.1038/ejhg.2011.264

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Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactylyPMID 22258522Read ↗

Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation.Semantic proximity Read ↗

Deletion of exon 4 of the PITX2 in a child with Axenfeld-Rieger syndrome.Semantic proximity Read ↗

A chromosomal 5q31.1 gain involving PITX1 causes Liebenberg syndrome.Semantic proximity Read ↗

Advances in the molecular genetics of non-syndromic polydactyly.Semantic proximity Read ↗

Pitx1 haploinsufficiency causes clubfoot in humans and a clubfoot-like phenotype in mice.Semantic proximity Read ↗

Polydactyly: how many disorders and how many genes? 2010 update.Semantic proximity Read ↗

PITX2 loss-of-function mutation contributes to tetralogy of FallotSemantic proximity Read ↗

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Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent CohortSemantic proximity Read ↗

PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in Split Hand/Foot MalformationSemantic proximity Read ↗

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