WAARDENBURG SYNDROME, TYPE IIA

Known as: WS2, Waardenburg Syndrome Type IIA, WS2A 
Waardenburg syndrome Type 2 caused by mutations in the MITF gene.
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Layer-by-layer stacking or lateral interfacing of atomic monolayers has opened up unprecedented opportunities to engineer two… (More)
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Highly Cited
2013
Highly Cited
2013
Geometrical confinement effect in exfoliated sheets of layered materials leads to significant evolution of energy dispersion in… (More)
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Highly Cited
2013
Highly Cited
2013
Individual monolayers of metal dichalcogenides are atomically thin two-dimensional crystals with attractive physical properties… (More)
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Highly Cited
2011
Highly Cited
2011
Two-dimensional (2D) nanomaterials have been receiving great attention in recent years because they show unusual physical… (More)
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Highly Cited
2010
Highly Cited
2010
Following the discovery of fullerenes in 1985, it was soon recognized that inorganic layered materials such as MoS2 and WS2 can… (More)
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Highly Cited
2000
Highly Cited
2000
Waardenburg syndrome (WS) is an autosomal dominant disorder with an incidence of 1 in 40 000 that manifests with sensorineural… (More)
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Highly Cited
1998
Highly Cited
1998
Waardenburg syndrome (WS) is a hereditary disorder that causes hypopigmentation and hearing impairment. Depending on additional… (More)
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Review
1997
Review
1997
Auditory-pigmentary syndromes are caused by physical absence of melanocytes from the skin, hair, eyes, or the stria vascularis of… (More)
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Highly Cited
1996
Highly Cited
1996
Hirschsprung disease (HSCR) or colonic agan-glionosis is a congenital disorder characterized by an absence of intramural ganglia… (More)
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Highly Cited
1994
Highly Cited
1994
Waardenburg syndrome type 2 (WS2) is a dominantly inherited syndrome of hearing loss and pigmentary disturbances. We recently… (More)
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