Literature DB >> 143443

Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype.

A Hagemeijer, E M Smit.   

Abstract

Cytogenetic analysis of a 6-year-old girl with moderate mental retardation revealed 46 chromosomes with a tandem translocation (21;21) resulting in a partial trisomy 21. Only the terminal band 21q22 was not in triplicate. G-, Q-, R-, and C-banding techniques and silver nitrate staining of the nucleolus organizer regions (NORs) were used to identify this chromosome fully. The phenotype of the patient was not typical for Down's syndrome, providing additional evidence that trisomy of band 21q22 is pathogenetic for the phenotype of Down's syndrome. This is also a new example in human pathology of a stable 'dicentric' chromosome in which one of the centromeric constrictions appears to be nonfunctional.

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Year:  1977        PMID: 143443     DOI: 10.1007/bf00295803

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  22 in total

1.  [A second example of telomeric fusion 2 X chromosomes].

Authors:  J Fraisse; C Laurent; N Collard; M C Biemont; B Dutrillaux
Journal:  Ann Genet       Date:  1975-12

2.  Dicentric human X chromosomes.

Authors:  A De la Chapelle; K Stenstrand
Journal:  Hereditas       Date:  1974       Impact factor: 3.271

3.  Partial trisomy 21.

Authors:  P Aula; J Leisti; H von Koskull
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

4.  Identification of G-group chromosomes involved in a G-G tandem-translocation by the giemsa-band technique.

Authors:  W Vogel
Journal:  Humangenetik       Date:  1972

5.  Abnormal X chromosomes in man: origin, behavior and effects.

Authors:  E Therman; K Patau
Journal:  Humangenetik       Date:  1974

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Authors:  J Lejeune; R Berger; O R Vidal; M O Réthoré
Journal:  Ann Genet       Date:  1965

7.  A simple R banding technic.

Authors:  R S Verma; H A Lubs
Journal:  Am J Hum Genet       Date:  1975-01       Impact factor: 11.025

8.  Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21.

Authors:  J D Williams; R L Summitt; P R Martens; R A Kimbrell
Journal:  Am J Hum Genet       Date:  1975-07       Impact factor: 11.025

9.  [Four new cases of X-autosome translocation in man (author's transl)].

Authors:  C Laurent; M C Biemont; B Dutrillaux
Journal:  Humangenetik       Date:  1975

10.  Late-replicating ring X-chromosomes identified by R-banding after BrdU pulse. Three new examples of mosaicism 45, XO/46, Xr(X).

Authors:  A Hagemeijer; J Hoovers; I Hasper-Voogt; T Von Ruhe-Zurcher; D Bootsma
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

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  37 in total

1.  Normal phenotype and partial trisomy for the G positive region of chromosome 21.

Authors:  A Daniel
Journal:  J Med Genet       Date:  1979-06       Impact factor: 6.318

2.  Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.

Authors:  Z Rahmani; J L Blouin; N Creau-Goldberg; P C Watkins; J F Mattei; M Poissonnier; M Prieur; Z Chettouh; A Nicole; A Aurias
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

3.  Overexpression of copper-zinc superoxide dismutase in trisomy 21.

Authors:  R De La Torre; A Casado; E López-Fernández; D Carrascosa; V Ramírez; J Sáez
Journal:  Experientia       Date:  1996-09-15

4.  Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17.

Authors:  S V Cheng; J H Nadeau; R E Tanzi; P C Watkins; J Jagadesh; B A Taylor; J L Haines; N Sacchi; J F Gusella
Journal:  Proc Natl Acad Sci U S A       Date:  1988-08       Impact factor: 11.205

5.  Familial 4.3 Mb duplication of 21q22 sheds new light on the Down syndrome critical region.

Authors:  Anne Ronan; Kerry Fagan; Louise Christie; Jeffrey Conroy; Norma J Nowak; Gillian Turner
Journal:  BMJ Case Rep       Date:  2009-06-04

6.  Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids.

Authors:  M L Van Keuren; P C Watkins; H A Drabkin; E W Jabs; J F Gusella; D Patterson
Journal:  Am J Hum Genet       Date:  1986-06       Impact factor: 11.025

7.  Concurrent psu dic(21)(q22.3) and t(13;17)(q14.1;p12) in a mosaic Down's syndrome patient: review of thirty-one similar dicentrics.

Authors:  Horacio Rivera; Ana I Vásquez-Velásquez
Journal:  J Genet       Date:  2014-04       Impact factor: 1.166

8.  Regional assignment of human liver-type 6-phosphofructokinase to chromosome 21q22.3 by using somatic cell hybrids and a monoclonal anti-L antibody.

Authors:  M Van Keuren; H Drabkin; I Hart; D Harker; D Patterson; S Vora
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

9.  Nucleotide sequence and expression of human chromosome 21-encoded superoxide dismutase mRNA.

Authors:  L Sherman; N Dafni; J Lieman-Hurwitz; Y Groner
Journal:  Proc Natl Acad Sci U S A       Date:  1983-09       Impact factor: 11.205

10.  Assignment of the gene for cytoplasmic superoxide dismutase (Sod-1) to a region of chromosome 16 and of Hprt to a region of the X chromosome in the mouse.

Authors:  U Francke; R T Taggart
Journal:  Proc Natl Acad Sci U S A       Date:  1979-10       Impact factor: 11.205

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