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Article

A new case of syndromic craniosynostosis with cryptic 19p13.2-p13.13 deletion.

American journal of medical genetics. Part A - 1 Nov 2009

Lysy Philippe A, Ravoet Marie, Wustefeld Sandrine, Bernard Pierre, Nassogne Marie-Cécile, Wyns Elisabeth, Sibille Catherine

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Share to Chromosome Deletion
Share to Comparative Genomic Hybridization
Share to Craniosynostoses
Share to In Situ Hybridization, Fluorescence

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19842200
DOI: 10.1002/ajmg.a.33056

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