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Literature DB >> 6453893

Hand abnormalities in the fetal hydantoin syndrome.

L Silver.

Abstract

Entities: Disease

Mesh：

Substances：
Phenytoin

Year: 1981 PMID： 6453893 DOI： 10.1016/s0363-5023(81)80082-2

Source DB: PubMed Journal: J Hand Surg Am ISSN： 0363-5023 Impact factor: 2.230

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1 in total

1. Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K⁺ channelopathies.

Authors: Karen W Gripp; Sarah F Smithson; Ingrid J Scurr; Julia Baptista; Anirban Majumdar; Germaine Pierre; Maggie Williams; Lindsay B Henderson; Ingrid M Wentzensen; Heather McLaughlin; Lisette Leeuwen; Marleen E H Simon; Ellen van Binsbergen; Mary Beth P Dinulos; Julie D Kaplan; Anne McRae; Andrea Superti-Furga; Jean-Marc Good; Kerstin Kutsche
Journal: Eur J Hum Genet Date: 2021-02-16 Impact factor: 4.246

1 in total

Hand abnormalities in the fetal hydantoin syndrome.

1. Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K+ channelopathies.

1. Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K⁺ channelopathies.