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5 in total

1. Universal acquired melanosis in siblings.

Authors: Snehansu Chakraborti; Tarak Nath Ghosh; Shankha Subhra Nag; Arvind Kumar Singh; Piyali Mitra
Journal: Indian J Pediatr Date: 2012-08 Impact factor: 1.967

2. Familial progressive hyper- and hypopigmentation: a report on a Chinese family and evidence for genetic heterogeneity.

Authors: Fang Xiao-Kai; He Yue-Xi; Li Yan-Jia; Chen Li-Rong; Wang He-Peng; Sun Qing
Journal: An Bras Dermatol Date: 2017 May-Jun Impact factor: 1.896

3. Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation.

Authors: Zhi-Qiang Wang; Lizhen Si; Quan Tang; Debao Lin; Zhangjie Fu; Jing Zhang; Bin Cui; Yufei Zhu; Xianghua Kong; Min Deng; Yu Xia; Heng Xu; Weidong Le; Landian Hu; Xiangyin Kong
Journal: Am J Hum Genet Date: 2009-04-16 Impact factor: 11.025

4. Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation.

Authors: Jianbo Wang; Weisheng Li; Naihui Zhou; Jingliu Liu; Shoumin Zhang; Xueli Li; Zhenlu Li; Ziliang Yang; Miao Sun; Min Li
Journal: BMC Med Genomics Date: 2021-01-06 Impact factor: 3.063

5. Familial progressive hyperpigmentation: a case report.

Authors: Monica Yadav; Sugandha Ghonasgi; Rohit Shah; S M Meghana
Journal: Case Rep Dent Date: 2012-04-18

5 in total