A Case Report On Waardenburg Syndrome : A Rare Genetic Disorder,IJAR - Indian Journal of Applied Research(IJAR) IJAR is a double reviewed monthly print ...
Waardenburg syndrome (WS) is a rare genetic disorder. Patients have heterochromia or eyes with iris of different color, increased inter-canthal distance, ...
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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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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, ...
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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 ...
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Waardenburg syndrome (WS) is a rare genetic disorder. Patients have heterochromia or eyes with iris of different color, increased inter-canthal distance, ...
Waardenburg syndrome (WS) is a rare genetic disorder first described in 1951 by Waardenburg as a combination of six chief characteristics: white forelock ...
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WAARDENBURG SYNDROME: ABOUT 7 CASES. by IJAR Indexing. International Journal of Advanced Research (IJAR). See Full PDF
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, ...
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Waardenburg syndrome (WS) is a rare genetic disorder. It is caused by ... International Journal of Advanced Research (IJAR). Download Free PDF View PDF.
