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Features of Turner's and DiGeorge's syndromes in a child with an X;22 translocation.

We describe the clinical and cytogenetic findings in an infant who presented with the features of both Turner's and DiGeorge's syndromes associated with a unique translocation between chromosomes X and 22.

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Autori principali: Pinto, M R, Leite, R P, Areias, A
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1989
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015761/
https://ncbi.nlm.nih.gov/pubmed/2614798
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