一个患有瓦登伯格综合征的英国家庭。 - Suppr

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超能文献

An English family with Waardenburg's syndrome.

作者信息

PARTINGTON M W

出版信息

Arch Dis Child. 1959 Apr;34(174):154-7. doi: 10.1136/adc.34.174.154.

DOI:10.1136/adc.34.174.154

PMID:13650669

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2012350/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76d7/2012350/8ef1e3de53c0/archdisch01611-0058-a.jpg

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本文引用的文献

A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.一种新的综合征，其合并了眼睑、眉毛和鼻根的发育异常，虹膜和头部毛发的色素沉着缺陷以及先天性耳聋。

Am J Hum Genet. 1951 Sep;3(3):195-253.

The first arch syndrome.第一鳃弓综合征

Arch Dis Child. 1958 Oct;33(171):477-86. doi: 10.1136/adc.33.171.477.

[Deaf-mutism with Waardenburg-Klein syndrome in children].

Ned Tijdschr Geneeskd. 1957 Jun 15;101(24):1120-1.

[A new form of congenital hereditary deafness (Waardenburg's syndrome)].[一种先天性遗传性耳聋的新形式（瓦登伯革氏综合征）]

Ned Tijdschr Geneeskd. 1952 Oct 11;96(41):2541-3.

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