[Complete deletion of the short arm of chromosome 18 and G-18 translocation with dyschromy and hypothyroidism].
作者信息
Malpuech G, Raynaud E J, Gaulme J, Godeneche P
出版信息
Arch Fr Pediatr. 1971 Oct;28(8):837-46.
PMID:5123541
Abstract
摘要
相似文献
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[Complete deletion of the short arm of chromosome 18 and G-18 translocation with dyschromy and hypothyroidism].[18号染色体短臂完全缺失及G-18易位伴色素异常和甲状腺功能减退]
Arch Fr Pediatr. 1971 Oct;28(8):837-46.
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引用本文的文献
1
[Ring chromosome 18. 18p-/18q- -deletion-syndrome].[环状染色体18。18p - /18q - 缺失综合征]
Humangenetik. 1972;15(4):289-318. doi: 10.1007/BF00281730.
2
Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns.通过G带模式鉴定克氏综合征的18 - 21易位
Humangenetik. 1974 Mar 28;21(4):323-9. doi: 10.1007/BF00273370.
3
A 46,XY, del(18)(pter leads to p1 100:) cebocephalic child from a 46,XX,t(12;18)(18pter leads to 18 p 1100:: 12qter leads to 12pter) normal parent.一名患有头面正中畸形的46,XY,del(18)(pter至p1 100:）患儿，其父母一方核型为正常的46,XX,t(12;18)(18pter至18 p 1100:: 12qter至12pter) 。
Hum Genet. 1976 Sep 10;34(1):103-6. doi: 10.1007/BF00284446.
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