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Article

Expanding the phenotype of 22q13.3 deletion: report of a case detected prenatally.

Prenatal diagnosis - 1 Oct 2008

Maitz Silvia, Gentilin Barbara, Colli Anna Maria, Rizzuti Tommaso, Brandolisio Emilia, Vetro Annalisa, Zuffardi Orsetta, Guerneri Silvana, Lalatta Faustina

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Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 22
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 18821718
DOI: 10.1002/pd.2110

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