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Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.

Chromosome analysis of an infant with characteristic features of trisomy 18 is presented. The chromosome complement contained a modal count of 47 but there was only one No. 18. In addition, there were two metacentric chromosomes of different sizes. The two metacentric chromosomes were identified by...

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Detalhes bibliográficos
Main Authors: Larson, L M, Wasdahl, W A, Saumur, J H, Coleman, M L, Jalal, S M
Formato: Artigo
Idioma:Inglês
Publicado em: 1978
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1012828/
https://ncbi.nlm.nih.gov/pubmed/633320
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