Results 61 to 70 of about 211 (109)

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

open access: yesAm J Hum Genet, 2000
Touraine RL   +16 more
europepmc   +1 more source

Waardenburg syndrome and myelomeningocele in a family. [PDF]

open access: yesJ Med Genet, 1993
Chatkupt S, Chatkupt S, Johnson WG.
europepmc   +1 more source

[Waardenburg syndrome].

open access: yesThe 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]

open access: yesBiol Open, 2016
Motohashi T   +9 more
europepmc   +1 more source

Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass. [PDF]

open access: yesBMC Dev Biol, 2009
Munroe RJ   +8 more
europepmc   +1 more source

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