Literature DB >> 2231652

Chromosome imbalance, normal phenotype, and imprinting.

L Bortotto1, E Piovan, R Furlan, H Rivera, O Zuffardi.   

Abstract

A duplication of the sub-bands 1q42.11 and 1q42.12 was found in a boy and his mother. The proband has short stature (around the 10th centile) but a normal phenotype and psychomotor development. His mother is also asymptomatic. We found 30 published cases of normal subjects with an imbalance of autosomal euchromatic material. In these cases the imbalance involved either only one G positive band or a G positive and a G negative band. Thus the absence of a phenotypic effect cannot always be ascribed to the deficiency in the G positive bands of coding DNA. Moreover, in some cases, the method of transmission of the chromosome abnormality was such that an imprinting effect could be postulated.

Entities:  

Mesh:

Year:  1990        PMID: 2231652      PMCID: PMC1017222          DOI: 10.1136/jmg.27.9.582

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


  31 in total

1.  Origin of a small metacentric chromosome: familial and cytogenic evidence.

Authors:  K M Taylor; H L Wolfinger; M G Brown; D L Chadwick
Journal:  Clin Genet       Date:  1975-11       Impact factor: 4.438

Review 2.  Mammalian chromosome banding--an expression of genome organization.

Authors:  W A Bickmore; A T Sumner
Journal:  Trends Genet       Date:  1989-05       Impact factor: 11.639

Review 3.  Aspects of evaluation, significance, and evolution of human C-band heteromorphism.

Authors:  B Erdtmann
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

4.  Two unusual G-band variants of the short arm of chromosome 9.

Authors:  G R Sutherland; H Eyre
Journal:  Clin Genet       Date:  1981-05       Impact factor: 4.438

5.  Prenatal detection of an accessory chromosome identified as an inversion duplication (15).

Authors:  G Stetten; B Sroka-Zaczek; V L Corson
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocation.

Authors:  L C Strong; V M Riccardi; R E Ferrell; R S Sparkes
Journal:  Science       Date:  1981-09-25       Impact factor: 47.728

7.  Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas.

Authors:  V M Riccardi; H M Hittner; U Francke; S Pippin; G P Holmquist; F L Kretzer; R Ferrell
Journal:  Clin Genet       Date:  1979-04       Impact factor: 4.438

8.  Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D.

Authors:  H Rivera; C Turleau; J de Grouchy; C Junien; S Despoisse; J M Zucker
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

Review 9.  Genomic imprinting and genetic disorders in man.

Authors:  W Reik
Journal:  Trends Genet       Date:  1989-10       Impact factor: 11.639

Review 10.  Chromosome maps of man and mouse. IV.

Authors:  A G Searle; J Peters; M F Lyon; J G Hall; E P Evans; J H Edwards; V J Buckle
Journal:  Ann Hum Genet       Date:  1989-05       Impact factor: 1.670

View more
  5 in total

1.  Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

Authors:  J C Barber; C A Joyce; M N Collinson; J C Nicholson; L R Willatt; H M Dyson; M S Bateman; A J Green; J R Yates; N R Dennis
Journal:  J Med Genet       Date:  1998-06       Impact factor: 6.318

2.  Trisomy 2q11.2-->q21.1 resulting from an unbalanced insertion in two generations.

Authors:  I A Glass; P Stormer; P T Oei; E Hacking; P D Cotter
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

Review 3.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

Review 4.  Chromosome abnormalities without phenotypic consequences.

Authors:  Małgorzata Kowalczyk; Małgorzata Srebniak; Agnieszka Tomaszewska
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

5.  Molecular analysis of three patients with interstitial deletions of chromosome band 14q31.

Authors:  B C Byth; M T Costa; I E Teshima; W G Wilson; N P Carter; D W Cox
Journal:  J Med Genet       Date:  1995-07       Impact factor: 6.318

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.