A new syndrome combining developmental anomalies o...[Am J Hum Genet. 1951]

SearchDatabase nameforSearch term

Your browser version may not work well with NCBI's Web applications. More information here...

Display Show

All: 1

Review: 0

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

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.

PMID: 14902764 [PubMed - indexed for MEDLINE]

PMCID: PMC1716407

Lineage-specific responses to reduced embryonic Pax3 expression levels.
Zhou HM, Wang J, Rogers R, Conway SJ. Dev Biol. 2008 Mar 15; 315(2):369-82. Epub 2007 Dec 27.

[Dev Biol. 2008]
WAARDENBURG'S SYNDROME.
Ray DK. Br J Ophthalmol. 1961 Aug; 45(8):568-9.

[Br J Ophthalmol. 1961]
Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4.
Bondurand N, Dastot-Le Moal F, Stanchina L, Collot N, Baral V, Marlin S, Attie-Bitach T, Giurgea I, Skopinski L, Reardon W, et al. Am J Hum Genet. 2007 Dec; 81(6):1169-85. Epub 2007 Oct 22.

[Am J Hum Genet. 2007]
» See all...

Your browsing activity is empty.

Activity recording is turned off.

Display Show