Results 161 to 170 of about 7,052 (205)

Genetic Variability of SOX10-Related Disorders within an Italian Family: Straddling the Line between Kallmann and Waardenburg Syndrome. [PDF]

Mol Syndromol
Graziani L, Carriero ML, Pozzi F, Minotti C, Andreadi A, Bellia A, Ruta R, Bengala M, Novelli A, Lauro D, Novelli G.   +10 more
europepmc   +1 more source

Waardenburg Syndrome Type 2 in Paediatrics: A Case Highlighting Diagnostic Complexities and the Efficacy of Cochlear Implantation. [PDF]

Indian J Otolaryngol Head Neck Surg
Kumar S, Natraj R, Dutta A.
europepmc   +1 more source

Waardenburg′s syndrome

Indian Journal of Ophthalmology, 1979
Boparai M, Sohi Balinder, Sohi A
doaj  

Waardenburg′s Syndrome

Indian Journal of Ophthalmology, 1957
Divekar M
doaj  

Waardenburg′s syndrome

Indian Journal of Ophthalmology, 1980
Joseph T, Chakravarthy K
doaj  

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Waardenburg syndrome

Journal of the European Academy of Dermatology and Venereology, 2001
AbstractWaardenburg syndrome (WS) is caused by autosomal dominant mutations, and is characterized by pigmentary anomalies and various defects of neural crest derived tissues. We report a very interesting case of type 1 WS (WS 1) in an adult who presented all the symptoms characteristic of this syndrome. One particularly important clinical feature of WS
P, Konno, H, Silm
openaire   +2 more sources

Waardenburg’s syndrome

The Indian Journal of Pediatrics, 1969
3 cases of Waardenburg’s syndrome in one family are reported. A brief description of the inheritance is given.
C M, Mahajan, S, Mehta
openaire   +2 more sources

Waardenburg syndrome

2021
18 months ...
openaire   +1 more source

Waardenburg syndrome

Indian Journal of Otolaryngology, 1972
A case of Waardenburg syndrome has been presented, who exhibited the various typical features and a generalized partial albinism in the form of scattered areas of vitiligo and poliosis.
G. M. Taneja, G. S. Bawa
openaire   +1 more source