Literature DB >> 933125

Pure partial trisomy for long arm of chromosome 9.

M Faed, J Robertson, S Brown, P J Smail, R D Muckhart.   

Abstract

A case of a 4-year-old boy with trisomy of the long arm of chromosome 9 is described (46,XY, der (9), t (9;9) (q32;q12)). The trisomy is probably the result of a translocation of the long arm of the chromosome from one homologue to the other in a parental gonad. The clinical features of the child which include severe developmental retardation, bird-like facies, tapered fingers, and flexion contractures of the legs are similar to those of the few cases described of trisomy of the whole chromosome.

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Year:  1976        PMID: 933125      PMCID: PMC1013401          DOI: 10.1136/jmg.13.3.239

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  14 in total

1.  47, XY, t(9pplus;11qplus) in a mlae infant with multiple malformations.

Authors:  N D Dinno; G L Silvey; B Weisskopf
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

2.  [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].

Authors:  M O Rethoré; H Hoehn; H D Rott; J Couturier; B Dutrillaux; J Lejeune
Journal:  Humangenetik       Date:  1973-04-16

3.  Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9.

Authors:  M Bobrow; K Madan; P L Pearson
Journal:  Nat New Biol       Date:  1972-07-26

4.  A rapid banding technique for human chromosomes.

Authors:  M Seabright
Journal:  Lancet       Date:  1971-10-30       Impact factor: 79.321

5.  Localization of heterochromatin in human chromosomes.

Authors:  F E Arrighi; T C Hsu
Journal:  Cytogenetics       Date:  1971

6.  Chromosome survey of a hospital for the mentally subnormal. 2. Autosome abnormalities.

Authors:  M S Newton; C Cunningham; P A Jacobs; W H Price; I A Fraser
Journal:  Clin Genet       Date:  1972       Impact factor: 4.438

7.  Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.

Authors:  P E Podruch; B Weisskopf
Journal:  J Pediatr       Date:  1974-07       Impact factor: 4.406

8.  Trisomy 9 mosaicism in a newborn infant with multiple malformations.

Authors:  P Bowen; K L Ying; G S Chung
Journal:  J Pediatr       Date:  1974-07       Impact factor: 4.406

9.  Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome.

Authors:  H Fujita; T Abe; K Yamamoto; J Furuyama
Journal:  Humangenetik       Date:  1974

10.  Four cases of 9p trisomy resulting from a balanced familial translocation (9:15) (q13;q11). Clinical picture and cytogenetic findings.

Authors:  J Zaremba; E Zdzienicka; I Glogowska; T Abramowicz; B Taracha
Journal:  J Ment Defic Res       Date:  1974-06
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  4 in total

1.  Cytogenetic and molecular analysis of a de novo tandem duplication of chromosome 21.

Authors:  J L Blouin; A Aurias; N Créau-Goldberg; F Apiou; C Alcaide-Loridan; A Bruel; M Prieur; J Kraus; J M Delabar; P M Sinet
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

Review 2.  Simultaneous trisomy 9q3 and monosomy 5p in two children with der(5),t(5;9)(p15.1;q34.13): report of an extended family.

Authors:  D Wellesley; I D Young; P Cooke; D F Callen; A Hockey
Journal:  J Med Genet       Date:  1988-10       Impact factor: 6.318

3.  Complete trisomy 9 in two liveborn infants.

Authors:  S Mantagos; J W McReynolds; M R Seashore; W R Breg
Journal:  J Med Genet       Date:  1981-10       Impact factor: 6.318

4.  A malformed girl with duplication of chromosome 9q.

Authors:  Y Nakahori; Y Nakagome
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318

  4 in total

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