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Prenatal diagnosis of Costello syndrome using 3D ultrasonography amniocentesis confirmation of the rare HRAS mutation G12D

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Bibliographic Details
Published in:	American journal of medical genetics. Part A 2009-04, Vol.149A (4), p.785-787
Main Authors:	Kuniba, Hideo, Pooh, Ritsuko K., Sasaki, Kensaku, Shimokawa, Osamu, Harada, Naoki, Kondoh, Tatsuro, Egashira, Masanori, Moriuchi, Hiroyuki, Yoshiura, Koh-ichiro, Niikawa, Norio
Format:	Article
Language:	English
Subjects:	Abnormalities, Multiple - diagnostic imaging Abnormalities, Multiple - genetics Amniocentesis Base Sequence Biological and medical sciences Complex syndromes Craniofacial Abnormalities - diagnostic imaging Craniofacial Abnormalities - genetics DNA Mutational Analysis Female Genes, ras Humans Infant, Newborn Male Medical genetics Medical sciences Mutation, Missense Phenotype Polyhydramnios - diagnostic imaging Polyhydramnios - genetics Pregnancy Syndrome Ultrasonography, Prenatal
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