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Article

A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defects.

American journal of human genetics - 1 Aug 1999

Saitta S C, McGrath J M, Mensch H, Shaikh T H, Zackai E H, Emanuel B S

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Topics

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Share to Adaptor Proteins, Vesicular Transport
Share to Cell Cycle Proteins
Share to Chromosome Banding
Share to Chromosome Deletion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 22

Share to Craniofacial Abnormalities

Share to Intracellular Signaling Peptides and Proteins

Share to Syndrome

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Identifiers

PMID: 10417299
DOI: 10.1086/302514
PMCID: PMC1377955

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