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. 1959 Apr;34(174):154–157. doi: 10.1136/adc.34.174.154

An English Family with Waardenburg's Syndrome

PMCID: PMC2012350 PMID: 13650669

154

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Fig. 2
on p.156

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

KEIZER D. P. R. Een nieuwe vorm van congenitale erfelijke doofheid (syndroom van Waardenburg). Ned Tijdschr Geneeskd. 1952 Oct 11;96(41):2541–2543. [PubMed] [Google Scholar]
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WAARDENBURG P. J. 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. Am J Hum Genet. 1951 Sep;3(3):195–253. [PMC free article] [PubMed] [Google Scholar]
WILDERVANCK L. S. Doofstomme kinderen met het syndroom van Waardenburg-Klein. Ned Tijdschr Geneeskd. 1957 Jun 15;101(24):1120–1121. [PubMed] [Google Scholar]

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