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

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Bibliographic Details
Published in:	American journal of medical genetics. Part A 2014-01, Vol.164A (1), p.264-266
Main Authors:	Sasaki, Aiko, Sumie, Masahiro, Wada, Seiji, Kosaki, Rika, Kurosawa, Kenji, Fukami, Maki, Sago, Haruhiko, Ogata, Tsutomu, Kagami, Masayo
Format:	Article
Language:	English
Subjects:	Abdominal wall Abnormalities, Multiple - diagnosis Abnormalities, Multiple - genetics Adult Chromosome Deletion Chromosomes, Human, Pair 14 Female Fetus Genetic Testing Genomic Imprinting Humans Phenotype Pregnancy Pregnancy Outcome Prenatal Diagnosis Uniparental Disomy - genetics
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