Results 131 to 140 of about 695 (177)

Dermoscopy of Amyloidosis Cutis Dyschromica.

Indian J Dermatol
Rane MC, Mahajan SA.
europepmc   +1 more source

A case of dyschromatosis universalis hereditaria.

Skin research, 1984
Shibuya, Kyoko, Kitano, Yukio
openaire   +1 more source

Leveraging genetics to understand ADAR1-mediated RNA editing in health and disease. [PDF]

Nat Rev Genet
Li JB, Walkley CR.
europepmc   +1 more source

Identification of the Mitf gene mutation causing congenital deafness and pigmentation disorders in porcupines using BSA-Seq. [PDF]

Sci Rep
Li K, Huo C, Long H, Tang K, Zhang S.
europepmc   +1 more source

A Case of Dyschromatosis Universalis Hereditaria

The Nishinihon Journal of Dermatology, 1983
TAKEHARA, Naohide, NAKAYAMA, Hidetoshi, MIHARA, Motoyuki, SHIMAO, Shuhei, MATSUMOTO, Isao   +4 more
openaire   +1 more source

Prediction of Skin Color Using Forensic DNA Phenotyping in Asian Populations: A Focus on Thailand. [PDF]

Biomolecules
Perez Palomeque G, Khacha-Ananda S, Monum T, Wunnapuk K.   +3 more
europepmc   +1 more source

Leukonychia Totalis: An Underreported Sign of Chronic Arsenicosis. [PDF]

Skin Appendage Disord
Bhoi AK, Gaurav V, Kushwaha S.
europepmc   +1 more source

Reticulate acropigmentation of Kitamura with café-au-lait macules: a rare case report. [PDF]

Front Med (Lausanne)
Gao B, Wang H, Fan Q, Cong L, Zhang G, Liu X.   +5 more
europepmc   +1 more source

Acquired brachial cutaneous dyschromatosis

, 2000
F.Rongioletti
core   +1 more source

Amyloidosis Cutis Dyschromica: A Rare Subtype of Primary Cutaneous Amyloidosis with Dermoscopy.

Indian J Dermatol
Priyadhashini BV, Agrawal I, Sahoo B, Mandal S.   +3 more
europepmc   +1 more source