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作者:Rai Ranju , Kaur Inderjeet , Handa Sanjeev ...
来源:[J].Indian Journal of Dermatology, Venereology and Leprology(IF 1.206), 2000, Vol.66 (3), pp.158
摘要:Dyschromatosis universalis hereditaria is a common disorder in Japan. We report a case in an Indian woman with no family history of the disorder.
作者:Rai Ranju , Kaur Inderjeet , Handa Sanjeev ...
来源:[J].Indian Journal of Dermatology, Venereology and Leprology(IF 1.206), 2000, Vol.66 (3), pp.158-159
摘要:Dyschromatosis universalis hereditaria is a common disorder in Japan. We report a case in an Indian woman with no family history of the disorder.
作者:Binitha M , Thomas Daisy , Asha L
来源:[J].Indian Journal of Dermatology, Venereology and Leprology(IF 1.206), 2006, Vol.72 (4), pp.300
摘要:... Dyschromatosis universalis hereditaria is an autosomal dominant genodermatosis, characterized by small hyperpigmented and hypopigmented macules, uniformly distributed over the entire body. The face is rarely involved, and the palms, soles, and mucous membranes are usually spa...
作者:Binitha M , Thomas Daisy , Asha L
来源:[J].Indian Journal of Dermatology, Venereology and Leprology(IF 1.206), 2006, Vol.72 (4), pp.300-302
摘要:... Dyschromatosis universalis hereditaria is an autosomal dominant genodermatosis, characterized by small hyperpigmented and hypopigmented macules, uniformly distributed over the entire body. The face is rarely involved, and the palms, soles, and mucous membranes are usually spa...
作者:Hong Liu , Yi Li , Ken Kwok Hon Hung ...
来源:[J].PLoS ONE(IF 3.73), 2017, Vol.9 (2)
摘要:As a genetic disorder of abnormal pigmentation, the molecular basis of dyschromatosis universalis hereditaria (DUH) had remained unclear until recently when ABCB6 was reported as a causative gene of DUH.We performed genome-wide linkage scan using Illumina Human 660W-Quad BeadChip...
作者:Ying-Xia Cui , Xin-Yi Xia , Yang Zhou ...
来源:[J].PLoS ONE(IF 3.73), 2017, Vol.8 (11)
摘要:Dyschromatosis universalis hereditaria (DUH) is a rare heterogeneous pigmentary genodermatosis, which was first described in 1933. The genetic cause has recently been discovered by the discovery of mutations in ABCB6. Here we investigated a Chinese family with typical features of...
作者:M Binitha , Daisy Thomas , L Asha
来源:[J].Indian Journal of Dermatology, Venereology, and Leprology(IF 1.206), 2006, Vol.72 (4), pp.300-302
摘要:... Dyschromatosis universalis hereditaria is an autosomal dominant genodermatosis, characterized by small hyperpigmented and hypopigmented macules, uniformly distributed over the entire body. The face is rarely involved, and the palms, soles, and mucous membranes are usually spa...
作者:Yi-Ying Chin , Gwo-Shing Chen , Stephen Chu-Sung Hu ...
来源:[J].Dermatologica Sinica(IF 0.218), 2011, Vol.29 (4), pp.137-141
摘要:Abstract(#br)Dyschromatosis universalis hereditaria (DUH) is a rare disease that is inherited both in autosomal dominant and autosomal recessive patterns. It is characterized by appearance of pinpoint to pea-sized hypo- and hyper-pigmented macules distributed in a reticulated pat...
作者:Yi-Ying Chin , Gwo-Shing Chen , Stephen Chu-Sung Hu ...
来源:[J].Zhōnghuá Pífūkē Yīxué Zázhì(IF 0.218), 2011, Vol.29 (4), pp.137-141
摘要:Dyschromatosis universalis hereditaria (DUH) is a rare disease that is inherited both in autosomal dominant and autosomal recessive patterns. It is characterized by appearance of pinpoint to pea-sized hypo- and hyper-pigmented macules distributed in a reticulated pattern over the...

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