Infancy- and childhood-onset dyschromatoses. - Wikidata - wikimedia - TriplyDB

Infancy- and childhood-onset dyschromatoses.

Infancy- and childhood-onset dyschromatoses.

http://www.wikidata.org/entity/Q37954716

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Dyschromatosis symmetrica hereditaria of late onset?Amyloidosis cutis dyschromica.Dyschromatosis Universalis Hereditaria with Oral Leukokeratosis--A Case of Mistaken Identity and Review of the Literature.Dyschromatosis universalis hereditaria with renal failure

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P2860

Infancy- and childhood-onset dyschromatoses.

http://www.wikidata.org/entity/Q37954716

description

article científic

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article scientifique

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artikel ilmiah

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Infancy- and childhood-onset dyschromatoses.

@en

Infancy- and childhood-onset dyschromatoses.

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type

label

Infancy- and childhood-onset dyschromatoses.

@en

Infancy- and childhood-onset dyschromatoses.

@nl

prefLabel

Infancy- and childhood-onset dyschromatoses.

@en

Infancy- and childhood-onset dyschromatoses.

@nl

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J.1365-2230.2011.04162.X

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Clinical and Experimental Dermatology

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Infancy- and childhood-onset dyschromatoses.

@en

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K Chanprapaph

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K Thadanipon

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V Vachiramon

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P2860

Dyschromatosis.

Cutaneous manifestations of nutritional deficiency.

Dyschromatosis universalis hereditaria: report of a case and review of the literature.

Hyperpigmentation in Chediak-Higashi syndrome.

The genetic basis of epidermolysis bullosa simplex with mottled pigmentation.

Reticulate pigmentary disorders--a review.

Epidermolysis bullosa simplex with mottled pigmentation.

Hereditary congenital hypopigmented and hyperpigmented macules.

"Cutis tricolor": congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: an unusual example of twin spotting?

Ectodermal dysplasia and abnormal thumbs.

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833-8, quiz 839

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scholarly article

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10.1111/J.1365-2230.2011.04162.X

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8

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