Literature DB >> 125542

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.

J D Williams, R L Summitt, P R Martens, R A Kimbrell.   

Abstract

This report deals with a reciprocal t(10;21) translocation which is observed in three generations of a family. Included are examples of the balanced translocation, adjacent-2 segregation producing three patients with trisomy of the distal long arm of chromosome 21 and the Down syndrome, and 3-1 disjunction producing trisomy of the proximal segment of chromosome 21 in a mildly mentally retarded boy without phenotypic features of the Down syndrome. These data provide evidence that the Down phenotype is attributable to trisomy of the distal long arm of chromosome 21.

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Year:  1975        PMID: 125542      PMCID: PMC1762808     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  18 in total

1.  A PARTIAL MONGOL.

Authors:  T DENT; J H EDWARDS; J D DELHANTY
Journal:  Lancet       Date:  1963-09-07       Impact factor: 79.321

2.  An unusual translocation in a case of Mongolism.

Authors:  H ZELLWEGER; K MIKAMO; G ABBO
Journal:  J Pediatr       Date:  1963-02       Impact factor: 4.406

3.  A chromosomal abnormality in a girl with some features of Down's syndrome (mongolism).

Authors:  J WARKANY; S W SOUKUP
Journal:  J Pediatr       Date:  1963-06       Impact factor: 4.406

4.  A new case of incomplete Down syndrome with partial trisomy 21.

Authors:  P L Giorgi; A Paci; M Ceccarelli; L Vizzoni
Journal:  Helv Paediatr Acta       Date:  1968-10

5.  Retardation in a child with an extra submetacentric chromosome fragment and partial mongolism.

Authors:  A S Dekaban; J Zelson
Journal:  J Ment Defic Res       Date:  1968-09

6.  Down's syndrome associated with a familial (21q-; 22q+) translocation.

Authors:  M M Cohen; R G Davidson
Journal:  Cytogenetics       Date:  1967

7.  Partial trisomy 21.

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

8.  [Two subterminal heterochromatin regions in a rare form of 21-21 translocation].

Authors:  M Bartsch-Sandhoff; H Schade
Journal:  Humangenetik       Date:  1973

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

Authors:  W Vogel
Journal:  Humangenetik       Date:  1972

10.  Dermatoglyphic nomogram for the diagnosis of Down's syndrome.

Authors:  T E Reed; D S Borgaonkar; P M Conneally; P Yu; W E Nance; J C Christian
Journal:  J Pediatr       Date:  1970-12       Impact factor: 4.406

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  31 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.  Partial trisomy 20 (20q13) and partial trisomy 21 (21pter leads to 21q21.3).

Authors:  O Sanchéz; P Mamunes; J J Yunis
Journal:  J Med Genet       Date:  1977-12       Impact factor: 6.318

3.  Indophenol-oxidase in patients with Down's syndrome due to simple trisomy and to translocation 21/22.

Authors:  J Kedziora; D Rozynkowa; M Kopff; J Jeske
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

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.  Human ETS2 gene on chromosome 21 is not rearranged in Alzheimer disease.

Authors:  N Sacchi; J Nalbantoglu; F R Sergovich; T S Papas
Journal:  Proc Natl Acad Sci U S A       Date:  1988-10       Impact factor: 11.205

6.  Partial trisomy 8q in half-sisters with distinct dysmorphic patterns not similar to the trisomy 8 mosaicism syndrome.

Authors:  A Schinzel
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

7.  Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen.

Authors:  D Weil; M G Mattei; E Passage; V C N'Guyen; D Pribula-Conway; K Mann; R Deutzmann; R Timpl; M L Chu
Journal:  Am J Hum Genet       Date:  1988-03       Impact factor: 11.025

8.  Fetal phenotype in a case of partial trisomy 21 and partial monosomy 22 detected prenatally.

Authors:  A M Migliorini; R Coco; T C De Negrotti; J M Sanchez; G Castineyra
Journal:  J Med Genet       Date:  1981-10       Impact factor: 6.318

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.  Down syndrome phenotypes: the consequences of chromosomal imbalance.

Authors:  J R Korenberg; X N Chen; R Schipper; Z Sun; R Gonsky; S Gerwehr; N Carpenter; C Daumer; P Dignan; C Disteche
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-24       Impact factor: 11.205

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