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Article

Prenatal genetic testing for a microdeletion at chromosome 14q32.2 imprinted region leading to UPD(14)pat-like phenotype.

American journal of medical genetics. Part A - 1 Jan 2014

Sasaki Aiko, Sumie Masahiro, Wada Seiji, Kosaki Rika, Kurosawa Kenji, Fukami Maki, Sago Haruhiko, Ogata Tsutomu, Kagami Masayo

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Share to Abnormalities, Multiple
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 14

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genomic Imprinting

Share to Pregnancy Outcome

Share to Prenatal Diagnosis

Share to Uniparental Disomy

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Identifiers

PMID: 24259232
DOI: 10.1002/ajmg.a.36185

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