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Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.

We have evaluated eight patients with pigmentary anomalies reminiscent of incontinentia pigmenti or hypomelanosis of Ito. All demonstrated abnormal lymphocyte karyotypes with chromosomal mosaicism in lymphocytes and/or skin fibroblasts. In seven the skin was darkly pigmented, and in all of these sev...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Thomas, I T, Frias, J L, Cantu, E S, Lafer, C Z, Flannery, D B, Graham, J G
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1989
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683341/
https://ncbi.nlm.nih.gov/pubmed/2667350
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