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Article

Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly.

Journal of medical genetics - 1 Apr 2005

Yatsenko S A, Cheung S W, Scott D A, Nowaczyk M J M, Tarnopolsky M, Naidu S, Bibat G, Patel A, Leroy J G, Scaglia F, Stankiewicz P, Lupski J R

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Share to Abnormalities, Multiple
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 9

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Craniofacial Abnormalities

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Share to In Situ Hybridization, Fluorescence

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Identifiers

PMID: 15805160
DOI: 10.1136/jmg.2004.028258
PMCID: PMC1736036

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Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly.PMID 15805160Read ↗

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