Hereditary hypomelanocytoses: the role of PAX3, SOX10, MITF, SNAI2, KIT, EDN3 and EDNRB genes Journal title: Advances in Hygiene and Experimental Medicine Authors: Michał Otręba, Maciej Miliński, Ewa Buszman, Dorota Wrześniok, Artur Beberok Subject(s): Medicine
Hipomelanocytozy dziedziczne: rola genów PAX3, SOX10, MITF, SNAI2, KIT, EDN3 i EDNRB Journal title: Advances in Hygiene and Experimental Medicine Authors: Michał Otręba, Maciej Miliński, Ewa Buszman, Dorota Wrześniok, Artur Beberok Subject(s): Medicine
Waardenburg Syndrome – A Case Report Journal title: Journal of Medical Science And clinical Research Authors: Dr Shabana Borate Subject(s):
Waardenburg Syndrome in an 8 Year Old African Child: Case Report Journal title: Journal of Advances in Medicine and Medical Research Authors: V. Odogu, I. O. Chukwuka, N. Chinawa Subject(s):
Waardenburg syndrome-associated focal segmental glomerulosclerosis: A rare presentation Journal title: Indian Journal of Child Health Authors: Murgu Sarasu J, Anju Aggarwal, Swati Bhayana, Aaradhana Singh Subject(s):
Waardenburg syndrome: A rare genetic disorder Journal title: International Journal of Medical Science and Innovative Research (IJMSIR) Authors: Dr. Rajbeer Singh Subject(s):
Waardenburg Syndrome Associated With Nephroticsyndrome and Hypothyroidism – A Rare Case Scenario Journal title: IOSR Journal of Dental and Medical Sciences (IOSR-JDMS) Authors: Dr.Sravya Ravi, Dr.P.V.V Satyanarayana Subject(s):
A STUDY OF OPHTHALMIC ASSOCIATION IN CHILDREN WITH SEVERE SENSORINEURAL DEAFNESS Journal title: Journal of Evidence Based Medicine and Healthcare Authors: Bharathi Mohan M., Kavitha K., Pramila B. Subject(s):
Waardenburg syndrome type 2 Journal title: Medical Journal Armed Forces Authors: Subhash Chandra Shaw Subject(s):
