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Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype.

A patient with a partial deletion (q23 leads to qter) of the long arm of chromosome 11 presented with craniosynostosis and syndactyly. These characteristics, which have not been previously reported with 11q--, expand the phenotype of this syndrome and emphasise the need for chromosome analysis with...

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Main Authors: Lippe, B M, Sparkes, R S, Fass, B, Neidengard, L
格式: Artigo
語言:Inglês
出版: 1980
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC1885929/
https://ncbi.nlm.nih.gov/pubmed/7205433
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