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11p13 deletion, Wilms' tumour, and aniridia: unusual genetic, non-ocular and ocular features of three cases.

Three cases of Wilms' tumour and sporadic aniridia were followed up for periods ranging from 32 months to seven years. All had a deletion of the short arm of the eleventh chromosome 11p13, including one case with mosaicism, a cytogenetic feature that has not been previously described in the Wil...

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Hlavní autoři: Jotterand, V, Boisjoly, H M, Harnois, C, Bigonesse, P, Laframboise, R, Gagné, R, St-Pierre, A
Médium: Artigo
Jazyk:Inglês
Vydáno: 1990
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1042214/
https://ncbi.nlm.nih.gov/pubmed/2168204
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