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Article

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

American journal of medical genetics. Part A - 15 Feb 2009

Kuniba Hideo, Pooh Ritsuko K, Sasaki Kensaku, Shimokawa Osamu, Harada Naoki, Kondoh Tatsuro, Egashira Masanori, Moriuchi Hiroyuki, Yoshiura Koh-ichiro, Niikawa Norio

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Share to Abnormalities, Multiple
Share to Amniocentesis
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Mutation, Missense

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Source

Identifiers

PMID: 18642361
DOI: 10.1002/ajmg.a.32335

Genes

HRAS

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Prenatal diagnosis of Costello syndrome using 3D ultrasonography amniocentesis confirmation of the rare HRAS mutation G12D.PMID 18642361Read ↗

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Costello syndrome with special cutaneous manifestations and HRAS G12D mutation: A case report and literature review.Semantic proximity Read ↗

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Fetal Phenotype of CHARGE Syndrome with a Molecular Confirmation: A Series of 13 Cases.Semantic proximity Read ↗

Costello syndrome with severe cutis laxa and mosaic HRAS G12S mutation.Semantic proximity Read ↗

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Molecular confirmation of HRAS p.G12S in siblings with Costello syndrome.Semantic proximity Read ↗

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