Fryns syndrome without deletion 16q.
作者信息
Coté G B, Papadakou-Lagoyanni S, Kairis M
出版信息
Ann Genet. 1980;23(3):171-2.
PMID:6968534
Abstract
Fryns and his colleagues described two children with a remarkably similar phenotype, and suggested their condition was due to a partial or total deletion of the long arm of chromosome 16 distal to band q21. We report the same phenotype in a boy whose blood karyotype was normal.
摘要
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Fryns syndrome without deletion 16q.
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引用本文的文献
1
Interstitial deletion for a region in the long arm of chromosome 16.16号染色体长臂某区域的间质缺失。
Hum Genet. 1983;65(2):134-8. doi: 10.1007/BF00286649.
2
Identical twins with deletion 16q syndrome: evidence that 16q12.2-q13 is the critical band region.患有16号染色体长臂缺失综合征的同卵双胞胎：证明16q12.2-q13是关键带区的证据。
Hum Genet. 1984;67(2):233-6. doi: 10.1007/BF00273010.
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