Waardenburg syndrome (WS) is a uncommon autosomal inherited and genetically heterogenous disorder .Patients have heterochromia or eyes with iris of different ...
Waardenburg syndrome (WS) is a rare genetic disorder. Patients have heterochromia or eyes with iris of different color, increased inter-canthal distance, ...
Missing: IJAR - Applied
Waardenburg Syndrome is a rare disorder of neural crest cell development. It is genetically inherited. Varying in prevalence from 1:42000 to 1:50,000, ...
Missing: IJAR - Applied
Waardenburg Syndrome Type Ii : A Case Report,IJAR - Indian Journal of Applied Research(IJAR) IJAR is a double reviewed monthly print journal that accepts ...
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In this report a case has been discussed of finding a 30 years old male patient with. Waardenburg syndrome. Keywords: Waardenburg syndrome, autosomal dominant ...
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A rare genetic mutation case report: Waardenburg syndrome type I. Case Report. Author Details : Gagandeep Kaur , Anureet Kaur , Mandeep Kaur* , Haramritpal ...
Missing: IJAR - Applied
Mar 4, 2021 · Waardenburg Syndrome Type 1 (WS1) is a rare hereditary disease, which is usually caused by the mutations of PAX3 (paired box 3).
Waardenburg syndrome (WS) is a rare genetic disorder. It is caused by multiple mutations affecting the melanocytes, leading to a multitude of skin, hair ...
We report an 11-month-old boy with WS1, one of four clinicat types of WS. He exhibited white forelock, hypopigmented macules and patches, heterochromia irides, ...
Missing: IJAR - Applied
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WAARDENBURG SYNDROME: ABOUT 7 CASES. by IJAR Indexing. International Journal of Advanced Research (IJAR). See Full PDF
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