Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain. [PDF]
Touraine RL +16 more
europepmc +1 more source
Waardenburg syndrome and myelomeningocele in a family. [PDF]
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]
Morell R +3 more
europepmc +1 more source
Life in the fast lane: mammalian disease models in the genomics era. [PDF]
Dow LE, Lowe SW.
europepmc +1 more source
Mouse and hamster mutants as models for Waardenburg syndromes in humans. [PDF]
Asher JH, Friedman TB.
europepmc +1 more source
Gene array analysis of neural crest cells identifies transcription factors necessary for direct conversion of embryonic fibroblasts into neural crest cells. [PDF]
Motohashi T +9 more
europepmc +1 more source
Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass. [PDF]
Munroe RJ +8 more
europepmc +1 more source
Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome. [PDF]
Santos H, Mateus J, Leal MJ.
europepmc +1 more source
Concise review of recent studies in vitiligo. [PDF]
Allam M, Riad H.
europepmc +1 more source

