Defect of neutrophil mobility with dominant inheritance in a family with Waardenburg's syndrome. [PDF]
Super M.
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The LKB1-SIK pathway: dysregulation in melanomagenesis and regulated use in skin cancer prevention [PDF]
The presence of dark melanin (eumelanin) within human epidermis represents one of the strongest predictors of skin cancer risk. Topical rescue of eumelanin synthesis, previously achieved in “redhaired” Mc1r-deficient mice, demonstrated significant ...
Mujahid, Nisma
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Waardenburg's syndrome. Report of a family. [PDF]
Cant JS, Martin AJ.
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Ontology-based methods for disease similarity estimation and drug repositioning [PDF]
Title from PDF of title page, viewed on October 2, 2012Dissertation advisor: Deendayal DinakarpandianVitaIncludes bibliographic references (p. 174-181)Thesis (Ph.D.)--School of Computing and Engineering and Dept. of Mathematics and Statistics. University
Mathur, Sachin
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Single-visit Feeding Obturator Fabrication in Infants with Cleft Lip and Palate: A Case Series and Narrative Review of Literature. [PDF]
Tirupathi SP, Ragulakollu R, Reddy V.
europepmc +1 more source
Waardenburg's syndrome and familial periodic paralysis. [PDF]
Tay CH.
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Waardenburg's syndrome in two siblings, both parents and their maternal grandmother. [PDF]
David TJ, Warin RP.
europepmc +1 more source
An English family with Waardenburg's syndrome. [PDF]
PARTINGTON MW.
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A Rare Co-occurrence of Intestinal Malrotation and Hirschsprung's Disease in a Neonate with 13q21.31q33.1 Interstitial Deletion Including the EDNRB Gene. [PDF]
Chatmethakul T +4 more
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