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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Larson, L M, Wasdahl, W A, Saumur, J H, Coleman, M L, Jalal, S M
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1978
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1012828/
https://ncbi.nlm.nih.gov/pubmed/633320
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