المؤلفون: Chen, Hongyu^{Aff1, Aff2}, Yang, Pingping^{Aff1, Aff2}, Yang, Dan, Wang, Dongsheng, Lu, Mao, Li, Yadong, Zhong, Zhiqiang, Zhang, Jing, Zeng, Zhen^{Aff1, Aff2}, Liu, Zhi, Zeng, Xiaohua, Jia, Xu, Xing, Qinghe, Zhou, Ding’an^{Aff2, IDs00109023022886_cor14}

المصدر: Journal of Molecular Medicine. 101(3):279-294

المؤلفون: Ranawaka, Ranthilaka Rasika^Aff3, Madarasinghe, Nayani P.^Aff3, Kannangara, Ajith Prasanna^Aff3, de Silva, Kanishka^Aff4

المساهمون: Smoller, Bruce, editor^Aff1, Bagherani, Nooshin, editor^Aff2

المصدر: Atlas of Dermatology, Dermatopathology and Venereology : Inflammatory Dermatoses. :991-1038

المؤلفون: An, Jingang^Aff4, Geng, Songmei^Aff4

المساهمون: Norman, Robert A., Series Editor^Aff1, Lotti, Torello M., editor^Aff2, Arcangeli, Fabio, editor^Aff3

المصدر: Clinical Cases in Adolescent Dermatology. :27-31

المؤلفون: Veena

المصدر: Pigment International, Vol 9, Iss 1, Pp 55-58 (2022)

مصطلحات موضوعية: dyschromatosis universalis hereditaria, keratoacanthoma, vendor dyschromatosis, Dermatology, RL1-803

وصف الملف: electronic resource

Relation: http://www.pigmentinternational.com/article.asp?issn=2349-5847;year=2022;volume=9;issue=1;spage=55;epage=58;aulast=; https://doaj.org/toc/2349-5847; https://doaj.org/toc/2349-5782

URL الوصول: https://doaj.org/article/3cfef83b7918404aabdbe9198c4c2fb8

المؤلفون: Min-Huei Lin, Pei-Chen Chou, I-Chen Lee, Syuan-Fei Yang, Hsin-Su Yu, Sebastian Yu

المصدر: Genes, Vol 14, Iss 6, p 1300 (2023)

مصطلحات موضوعية: dermatopathia pigmentosa reticularis, Dowling-Degos disease, dyschromatosis symmetrica hereditaria, dyschromatosis universalis hereditaria, dyskeratosis congenita, Naegeli–Franceschetti–Jadassohn syndrome, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4425/14/6/1300; https://doaj.org/toc/2073-4425

URL الوصول: https://doaj.org/article/71b6766ed64341de94d1bc2e63dd9746

المؤلفون: Pradhan, Swetalina^Aff5, Sahu, Kananbala^Aff6

المساهمون: Norman, Robert A., Series Editor^Aff1, Kothiwala, Sunil, editor^Aff2, Kumar Tiwary, Anup, editor^Aff3, Kumar, Piyush, editor^Aff4

المصدر: Clinical Cases in Disorders of Melanocytes. :157-160

المؤلفون: Lu Cao, Ruixue Zhang, Liang Yong, Shirui Chen, Hui Zhang, Weiwei Chen, Qiongqiong Xu, Huiyao Ge, Yiwen Mao, Qi Zhen, Yafen Yu, Xia Hu, Liangdan Sun

المصدر: BMC Medical Genomics, Vol 14, Iss 1, Pp 1-8 (2021)

مصطلحات موضوعية: ABCB6 gene, Dyschromatosis universalis hereditaria, Mutation, SASH1 gene, Internal medicine, RC31-1245, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1755-8794

URL الوصول: https://doaj.org/article/a4b9f9a6723749759c070dd51d7d7d14

المؤلفون: Meshal Mohammad Alhameedy, MD

المصدر: JAAD Case Reports, Vol 11, Iss , Pp 23-25 (2021)

مصطلحات موضوعية: dyschromatosis symmetrica hereditaria, dyschromatosis universalis hereditaria, hyper- and hypopigmentation, Dermatology, RL1-803

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2352512621001788; https://doaj.org/toc/2352-5126

URL الوصول: https://doaj.org/article/7e352eaee57e4b4cad50bc9093d3f64e

المؤلفون: Cao, Lu^{Aff1, Aff2, Aff3, Aff4, Aff5}, Zhang, Ruixue^{Aff1, Aff2, Aff3, Aff4, Aff5}, Yong, Liang^{Aff1, Aff2, Aff3, Aff4, Aff5}, Chen, Shirui^{Aff1, Aff2, Aff3, Aff4, Aff5}, Zhang, Hui^{Aff1, Aff2, Aff3, Aff4, Aff5}, Chen, Weiwei^{Aff1, Aff2, Aff3, Aff4, Aff5}, Xu, Qiongqiong^{Aff1, Aff2, Aff3, Aff4, Aff5}, Ge, Huiyao^{Aff1, Aff2, Aff3, Aff4, Aff5}, Mao, Yiwen^{Aff1, Aff2, Aff3, Aff4, Aff5}, Zhen, Qi^{Aff1, Aff2, Aff3, Aff4, Aff5}, Yu, Yafen^{Aff1, Aff2, Aff3, Aff4, Aff5}, Hu, Xia^{Aff1, Aff2, Aff3, Aff4, Aff5}, Sun, Liangdan^{Aff1, Aff2, Aff3, Aff4, Aff5}

المصدر: BMC Medical Genomics. 14(1)

المؤلفون: Sardar, Swapan Kumar, Das, Anupam, Bandyopadhyay, Debabrata Bandyopadhyay

المصدر: Dermatology Online Journal. 22(9)

مصطلحات موضوعية: Dyschromatosis universalis hereditaria, pigmentation disorder

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/24p9j62b