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Char syndrome, a familial form of patent ductus arteriosus, with a new finding: hypoplasia [corrected] of the 3rd finger.

Anadolu kardiyoloji dergisi : AKD = the Anatolian journal of cardiology - 1 Sept 2012

Babaoğlu Kadir, Oruç Meral, Günlemez Ayla, Gelb Bruce D

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 22728731
DOI: 10.5152/akd.2012.165

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Related research

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Char syndrome, a familial form of patent ductus arteriosus, with a new finding: hypoplasia [corrected] of the 3rd finger.PMID 22728731Read ↗

Familial patent ductus arteriosus: a further case of CHAR syndrome.Semantic proximity Read ↗

Char Syndrome, an Inherited Disorder With Patent Ductus Arteriosus, Maps to Chromosome 6p12-p21Semantic proximity Read ↗

Familial patent ductus arteriosus and bicuspid aortic valve with hand anomalies: a novel heart-hand syndrome.Semantic proximity Read ↗

Char syndrome: a new family and review of the literature emphasising the presence of symphalangism and the variable phenotype.Semantic proximity Read ↗

Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus.Semantic proximity Read ↗

Familial nonsyndromic patent ductus arteriosus caused by mutations in TFAP2B.Semantic proximity Read ↗

Novel TFAP2B mutation in nonsyndromic patent ductus arteriosus.Semantic proximity Read ↗

Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation.Semantic proximity Read ↗

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