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Article

Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome.

Journal of medical genetics - 1 Aug 2003

Zweier C, Temple I K, Beemer F, Zackai E, Lerman-Sagie T, Weschke B, Anderson C E, Rauch A

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Identifiers

PMID: 12920073
DOI: 10.1136/jmg.40.8.601
PMCID: PMC1735564

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Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome.PMID 12920073Read ↗

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