Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

1997
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 1
2004 1
2013 1
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Search Results

3 results

Results by year

Filters applied: . Clear all
Page 1
Melanocytes and the microphthalmia transcription factor network.
Steingrímsson E, Copeland NG, Jenkins NA. Steingrímsson E, et al. Annu Rev Genet. 2004;38:365-411. doi: 10.1146/annurev.genet.38.072902.092717. Annu Rev Genet. 2004. PMID: 15568981 Review.
The human homologue of MITF is mutated in patients with the pigmentary and deafness disorder Waardenburg Syndrome Type 2A (WS2A). The mouse Mitf mutations therefore serve as a model for the study of this human disease. ...
The human homologue of MITF is mutated in patients with the pigmentary and deafness disorder Waardenburg Syndrome Type
[Hereditary hypomelanocytoses: the role of PAX3, SOX10, MITF, SNAI2, KIT, EDN3 and EDNRB genes].
Otręba M, Miliński M, Buszman E, Wrześniok D, Beberok A. Otręba M, et al. Postepy Hig Med Dosw (Online). 2013 Nov 26;67:1109-18. doi: 10.5604/17322693.1077722. Postepy Hig Med Dosw (Online). 2013. PMID: 24379252 Free article. Review. Polish.
For example, mutations of the MITF gene cause Waardenburg syndrome type 2A as well as Tietz syndrome. It has also been demonstrated that mutations of different genes may cause an identical syndrome. ...
For example, mutations of the MITF gene cause Waardenburg syndrome type 2A as well as Tietz syndrome. It has als …