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

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

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Presumptive long arm deletion of chromosome 8: a new syndrome?

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3

Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn--karyotype: 46,XX,del(2)(q21;q24).

Hum Genet. 1977 Nov 10;39(2):233-8. doi: 10.1007/BF00287018.

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Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).

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5

Chromosome 6q- and associated malformations.

Ann Genet. 1978 Dec;21(4):223-5.

6

Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newborns.

Ann Genet. 1985;28(4):248-50.

7

Deletion of chromosome region 18q21.1 --> 18q21.3 in a patient without clinical features of the 18q- phenotype.

Am J Med Genet A. 2003 Jun 15;119A(3):356-9. doi: 10.1002/ajmg.a.10266.

8

[Interstitial deletion of the long arm of one 11 chromosome].

Ann Genet. 1975 Mar;18(1):61-3.

9

Distal deletion of the short arm of chromosome No. 10: a case report.

Jinrui Idengaku Zasshi. 1983 Dec;28(4):291-6. doi: 10.1007/BF01876793.

10

De novo interstitial deletion of the long arm of chromosome 2 in a malformed newborn with a karyotype: 46,XY,del(2)(q12q14).

Acta Paediatr Scand. 1983 Jul;72(4):631-3. doi: 10.1111/j.1651-2227.1983.tb09785.x.

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1

"Microcytogenetics" and Langer-Giedion syndrome.

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

2

Langer-Giedion syndrome with and without del 8q. assignment of critical segment to 8q23.

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

3

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

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

4

Langer-Giedion syndrome and deletion of the long arm of chromosome 8. Confirmation of the critical segment to 8q23.

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

5

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

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

6

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).

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

7

Microcytogenetics 1984.

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

8

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

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

9

Human chromosome 8.

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

本文引用的文献

1

[Ring chromosome 8 (46,XY, 8 r) in a boy with debility (author's transl)].

Klin Padiatr. 1973 May;185(3):187-91.

2

A new chromosome deletion syndrome. Report of a patient with a 46,XY,8p- chromosome constitution.

Clin Genet. 1976 Mar;9(3):289-301. doi: 10.1111/j.1399-0004.1976.tb01577.x.

3

[Partial deletion of the short arm of chromosome 8].

Ann Genet. 1975 Dec;18(4):251-5.

4

Deletion of the long arm of chromosome 8 resulting from a de novo translocation t(4;8) (q13;q213).

Hum Genet. 1977 Sep 22;38(2):125-30. doi: 10.1007/BF00527393.

5

Small structural changes of chromosome 8. Two cases with evidence for deletion.

Hum Genet. 1977 Aug 31;38(1):113-21. doi: 10.1007/BF00295814.

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