一名患有先天性青光眼、唇腭裂的儿童存在涉及3号、11号和14号染色体的复杂易位，并伴有中间缺失，即del(14)(q13q22)。 - Suppr

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A complex translocation involving chromosomes 3,11, and 14 with an interstitial deletion, del(14) (q13q22) in a child with congenital glaucoma and cleft lip and palate.

作者信息

Buchanan P D, Rao K W, Doerr C L, Aylsworth A S

出版信息

Birth Defects Orig Artic Ser. 1978;14(6C):317-22.

PMID:728587

Abstract

摘要

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A complex translocation involving chromosomes 3,11, and 14 with an interstitial deletion, del(14) (q13q22) in a child with congenital glaucoma and cleft lip and palate.一名患有先天性青光眼、唇腭裂的儿童存在涉及3号、11号和14号染色体的复杂易位，并伴有中间缺失，即del(14)(q13q22)。

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引用本文的文献

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