Langer-Giedion syndrome and deletion of the long arm of chromosome 8.

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作者信息

Fryns J P, Logghe N, van Eygen M, Van den Berghe H

出版信息

Hum Genet. 1981;58(2):231-2. doi: 10.1007/BF00278720.

DOI:10.1007/BF00278720

PMID:6974680

Abstract

摘要

相似文献

Langer-Giedion syndrome and deletion of the long arm of chromosome 8.

Hum Genet. 1981;58(2):231-2. doi: 10.1007/BF00278720.

Langer-Giedion syndrome and deletion of the long arm of chromosome 8. Confirmation of the critical segment to 8q23.朗格-吉迪恩综合征与8号染色体长臂缺失。8q23关键区段的确认。

Hum Genet. 1983;64(2):194-5. doi: 10.1007/BF00327126.

Terminal or interstitial deletion in chromosome 8 long arm in Langer-Giedion syndrome (TRP II syndrome)?朗格-吉迪恩综合征（TRP II综合征）中8号染色体长臂的末端或中间缺失？

Hum Genet. 1983;64(2):163-6. doi: 10.1007/BF00327117.

The critical segment for the Langer-Giedion syndrome: 8q24.11----q24.12.

Ann Genet. 1985;28(4):224-7.

Langer-Giedion syndrome with and without del 8q. assignment of critical segment to 8q23.伴或不伴8q缺失的朗格-吉迪恩综合征。关键片段定位于8q23。

Hum Genet. 1982;62(3):183-7. doi: 10.1007/BF00333515.

Langer-Giedion syndrome with interstitial 8q-deletion.伴有8号染色体长臂间质性缺失的朗格-吉迪恩综合征。

Am J Med Genet. 1982 Mar;11(3):353-8. doi: 10.1002/ajmg.1320110312.

No chromosome deletion found on prometaphase banding in two cases of Langer-Giedion syndrome.

Am J Med Genet. 1982 Nov;13(3):345-7. doi: 10.1002/ajmg.1320130322.

Tricho-rhino-phalangeal syndrome type I with severe mental retardation due to interstitial deletion of 8q23.3-24.13.由于8q23.3 - 24.13间质性缺失导致的伴有严重智力障碍的I型毛发 - 鼻 - 指（趾）综合征

Am J Med Genet. 1989 Jan;32(1):133-5. doi: 10.1002/ajmg.1320320128.

Familial syndrome with some features of the Langer-Giedion syndrome, and paracentric inversion of chromosome 8, inv 8 (q11.23----q21.1).

Clin Genet. 1985 Jun;27(6):600-5. doi: 10.1111/j.1399-0004.1985.tb02045.x.

Langer-Giedion syndrome and additional congenital malformations with interstitial deletion of the long arm of chromosome 8 46, XY, del 8 (q 13-22).朗格-吉迪恩综合征及伴有8号染色体长臂间质性缺失的其他先天性畸形 46，XY，del 8（q13-22）

Clin Genet. 1980 Aug;18(2):142-6. doi: 10.1111/j.1399-0004.1980.tb01025.x.

引用本文的文献

"Microcytogenetics" and Langer-Giedion syndrome.“微细胞遗传学”与朗格-吉迪恩综合征。

J Med Genet. 1982 Oct;19(5):390-1. doi: 10.1136/jmg.19.5.390-a.

Langer-Giedion syndrome with and without del 8q. assignment of critical segment to 8q23.伴或不伴8q缺失的朗格-吉迪恩综合征。关键片段定位于8q23。

Hum Genet. 1982;62(3):183-7. doi: 10.1007/BF00333515.

Langer-Giedion syndrome and deletion of the long arm of chromosome 8. Confirmation of the critical segment to 8q23.朗格-吉迪恩综合征与8号染色体长臂缺失。8q23关键区段的确认。

Hum Genet. 1983;64(2):194-5. doi: 10.1007/BF00327126.

Terminal or interstitial deletion in chromosome 8 long arm in Langer-Giedion syndrome (TRP II syndrome)?朗格-吉迪恩综合征（TRP II综合征）中8号染色体长臂的末端或中间缺失？

Hum Genet. 1983;64(2):163-6. doi: 10.1007/BF00327117.

Langer-Giedion syndrome, in a child with complex structural aberration of chromosome 8.

Hum Genet. 1983;63(2):178-82. doi: 10.1007/BF00291541.

Two cases of the Langer-Giedion syndrome with the same interstitial deletion of the long arm of chromosome 8: 46, XY or XX, del (8) (q23.3q24.13).两例患有相同8号染色体长臂间质性缺失的朗格-吉迪恩综合征：46，XY或XX，del(8)(q23.3q24.13) 。

Hum Genet. 1983;64(1):90-3. doi: 10.1007/BF00289486.

Microcytogenetics 1984.

Experientia. 1986 Oct 15;42(10):1090-7. doi: 10.1007/BF01941282.

8q24.12 Interstitial deletion in trichorhinophalangeal syndrome type I.

Hum Genet. 1986 Oct;74(2):188-9. doi: 10.1007/BF00282091.

Human chromosome 8.人类8号染色体。

J Med Genet. 1988 Nov;25(11):721-31. doi: 10.1136/jmg.25.11.721.

本文引用的文献

Chromosome deletion and multiple cartilaginous exostoses.染色体缺失与多发性骨软骨瘤

Eur J Pediatr. 1980 Mar;133(2):163-6. doi: 10.1007/BF00441586.

Clin Genet. 1980 Aug;18(2):142-6. doi: 10.1111/j.1399-0004.1980.tb01025.x.

Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21).

Hum Genet. 1979 Apr 17;48(1):127-30. doi: 10.1007/BF00273286.

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