Waardenburg syndrome (WS) is a uncommon autosomal inherited and genetically heterogenous disorder .Patients have heterochromia or eyes with iris of different ...
Waardenburg syndrome is a rare genetic disorder characterized by varying degree of deafness associated with pigmentary anomaly and defects of neural crest ...
Missing: IJAR - Applied Research
... <journal-meta> <journal-id journal-id-type="publisher">IJAR</journal-id> <journal-title>Indian Journal of Applied Research ... A CASE REPORT ON WAARDENBURG ...
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
Dec 15, 2020 · Waardenburg syndrome is a genetic disorder named after a Dutch ophthalmologist who has first described the triad of hearing loss, ...
Neural tube defects in Waardenburg syndrome: A case report and review of the literature. ... 2023, INDIAN JOURNAL OF APPLIED RESEARCH, p. 64-65. Crossref ...
A rare genetic mutation case report: Waardenburg syndrome type I. Case Report. Author Details : Gagandeep Kaur , Anureet Kaur , Mandeep Kaur* , Haramritpal ...
Missing: IJAR - Applied
Waardenburg syndrome (WS) is a rare genetic disorder characterized by congenital sensorineural hearing loss and pigmentary abnormalities of the hair, skin ...
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Waardenburg syndrome (WS) is a rare autosomally inherited and genetically heterogeneous disorder of neural crest cell development with distinct cutaneous ...
Missing: IJAR - Applied
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