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Partial trisomy 18 in a family with a translocation (18;21)(q21;q22).

A family is described in which 2 sibs had similar congenital abnormalities. Chromosome investigation of the mother and another child disclosed they were carriers of a translocation t(18;21)(q21;q22). The karyotype of one of the abnormal infants was determined and was found to be consistent with part...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Niazi, M, Coleman, D V, Saldaña-Garcia, P
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1978
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1013665/
https://ncbi.nlm.nih.gov/pubmed/641950
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