Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

Wilms tumor of the kidney occurs with increased frequency in association with two clinically and cytogenetically distinct congenital syndromes, the Wiedemann-Beckwith syndrome (WBS) and the triad of aniridia, genitourinary anomalies, and mental retardation (WAGR). Constitutional deletions in the lat...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Koufos, A, Grundy, P, Morgan, K, Aleck, K A, Hadro, T, Lampkin, B C, Kalbakji, A, Cavenee, W K
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1989
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715635/
https://ncbi.nlm.nih.gov/pubmed/2539717
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