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A report of a child with a deletion (9)(q34.3): a recognisable phenotype?

We report a case of a male infant who presented with congenital anomalies and was found to have a de novo deletion in the terminal region of the long arm of chromosome 9. He died at the age of 17 weeks of cardiorespiratory failure owing to RSV positive bronchiolitis. A review of previously published...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Ayyash, H, Mueller, R, Maltby, E, Horsfield, P, Telford, N, Tyler, R
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1997
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051009/
https://ncbi.nlm.nih.gov/pubmed/9222977
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