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MEDICINA-LITHUANIA, ISSN 1010-660X, 07/2019, Volume 55, Issue 7, p. 345
Congenital sensorineural hearing loss may occur in association with inborn pigmentary defects of the iris, hair, and skin. These conditions, named... 
15q13.3 deletion | genodermatoses | PHENOTYPE | genetic skin disorders | neurocristopathies | auditory-pigmentary disorders | multilocus syndrome | HOMOZYGOSITY | MEDICINE, GENERAL & INTERNAL | piebaldism | KIT | DEAFNESS | 15Q13.3
Journal Article
MEDICINA-LITHUANIA, ISSN 1010-660X, 03/2019, Volume 55, Issue 3, p. 78
The term congenital hypopigmentary disorders refers to a wide group of heterogeneous hereditary diseases, clinically characterized by inborn pigmentary defects... 
GRISCELLI-SYNDROME | MEDICINE, GENERAL & INTERNAL | pigmentation disorders | genodermatoses | genetic skin disorders | gray hair syndromes | griscelli syndrome | congenital hypopigmentary disorders
Journal Article
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, ISSN 1610-0379, 03/2018, Volume 16, Issue 3, pp. 360 - 363
Journal Article
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, ISSN 1610-0379, 03/2018, Volume 16, Issue 3, pp. 360 - 364
Journal Article
Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia, 10/2018
Journal Article
ISSN 0340-3696, 2018
Germline mutations on the CDKN2A gene, the most important known genetic factors associated with cutaneous melanomas (CMs), predispose carriers to multiple... 
Journal Article
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