Results 101 to 110 of about 433 (176)

Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain. [PDF]

Am J Hum Genet, 2000
Touraine RL, Attié-Bitach T, Manceau E, Korsch E, Sarda P, Pingault V, Encha-Razavi F, Pelet A, Augé J, Nivelon-Chevallier A, Holschneider AM, Munnes M, Doerfler W, Goossens M, Munnich A, Vekemans M, Lyonnet S.   +16 more
europepmc   +1 more source

Waardenburg syndrome and myelomeningocele in a family. [PDF]

J Med Genet, 1993
Chatkupt S, Chatkupt S, Johnson WG.
europepmc   +1 more source

The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1). [PDF]

J Med Genet, 1997
Morell R, Friedman TB, Asher JH, Robbins LG.   +3 more
europepmc   +1 more source

Life in the fast lane: mammalian disease models in the genomics era. [PDF]

Cell, 2012
Dow LE, Lowe SW.
europepmc   +1 more source

Mouse and hamster mutants as models for Waardenburg syndromes in humans. [PDF]

J Med Genet, 1990
Asher JH, Friedman TB.
europepmc   +1 more source

Cytogenetic, histologic and anatomic studies of heterochromia iridis in the restricted rat / [PDF]

, 1972
Harkins, Rosemary K.,
core  

[Waardenburg syndrome].

The Pan African medical journal, 2016
Mahfoudhi, Madiha, Khamassi, Khaled
openaire   +3 more sources

Gene array analysis of neural crest cells identifies transcription factors necessary for direct conversion of embryonic fibroblasts into neural crest cells. [PDF]

Biol Open, 2016
Motohashi T, Watanabe N, Nishioka M, Nakatake Y, Yulan P, Mochizuki H, Kawamura Y, Ko MS, Goshima N, Kunisada T.   +9 more
europepmc   +1 more source

Pax and vertebrate development [PDF]

, 1996
Gruss, P., Wehr, R.
core   +1 more source

A molecular investigation of Waardenburg syndrome in Southern Africa [PDF]

, 2017
Butt, Jennifer Leigh
core