Literature DB >> 4837287

A family with two translocations and a polymorphism involving chromosome 14.

P A Jacobs, K E Buckton, S Christie, M Newton, D Matthew.   

Abstract

Mesh：

Year:  1974        PMID： 4837287      PMCID： PMC1013089          DOI： 10.1136/jmg.11.1.65

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


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  7 in total

1.  Down's syndrome with a familial D/D reciprocal translocation and a G/G chromosome.

Authors:  H B Marsden; R I Mackay; A Murray; H E Ward
Journal:  J Med Genet       Date:  1966-03       Impact factor: 6.318

2.  An analysis of the break points of structural rearrangements in man.

Authors:  P A Jacobs; K E Buckton; C Cunningham; M Newton
Journal:  J Med Genet       Date:  1974-03       Impact factor: 6.318

3.  A simple technique for demonstrating centromeric heterochromatin.

Authors:  A T Sumner
Journal:  Exp Cell Res       Date:  1972-11       Impact factor: 3.905

4.  New technique for distinguishing between human chromosomes.

Authors:  A T Sumner; H J Evans; R A Buckland
Journal:  Nat New Biol       Date:  1971-07-07

5.  Distinguishing between the chromosomes involved in Down's syndrome (trisomy 21) and cronic myeloid leukaemia (Ph1) by fluorescence.

Authors:  M L O'Riordan; J A Robinson; K E Buckton; H J Evans
Journal:  Nature       Date:  1971-03-19       Impact factor: 49.962

6.  The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography.

Authors:  M M Cohen
Journal:  Ann Genet       Date:  1971-06

7.  Occurrence of a presumptive C-B translocation carrier [46,XY,t (? Cp-; Bp+)] in a family of D-G translocation carriers [45,D-,G-,t (DqGq)+].

Authors:  G H Thomas; W B Bias
Journal:  J Med Genet       Date:  1969-12       Impact factor: 6.318
  7 in total
  8 in total

1.  Aspermia, associated with a presumably balanced X/autosomal translocation karyotype 46, Y, t (X;5) (q28;q11).

Authors:  S Stengel-Rutkowski; H Zankl; A Rodewald; S Scharrer; J P Chaudhuri; K D Zang
Journal:  Hum Genet       Date:  1976-01-28       Impact factor: 4.132

Review 2.  Are double translocations double trouble?

Authors:  S M Bowser-Riley; M J Griffiths; M R Creasy; P A Farndon; K E Martin; D A Thomson; S A Larkins; R A Johnson; J L Watt
Journal:  J Med Genet       Date:  1988-05       Impact factor: 6.318

3.  Parental origin of de novo chromosome rearrangements.

Authors:  J Chamberlin; R E Magenis
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

4.  Unstable familial translocations: A t(11;22)mat inherited as a t(11;15).

Authors:  D J Tomkins
Journal:  Am J Hum Genet       Date:  1981-09       Impact factor: 11.025

5.  A 5;7, 5;12 double reciprocal translocation in a normal mother and a 5;7 translocation with a recombinant chromosome 5 in her normal child.

Authors:  A Tabor; L K Jensen; C Lundsteen; E Niebuhr
Journal:  J Med Genet       Date:  1981-08       Impact factor: 6.318

6.  A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members.

Authors:  A Smith; M Noel
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

7.  Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome.

Authors:  J B Bijlsma; H F de France; L M Bleeker-Wagemakers; P F Dijkstra
Journal:  Hum Genet       Date:  1978-01-19       Impact factor: 4.132

8.  Chromosomal instability in first trimester miscarriage: a common cause of pregnancy loss?

Authors:  Philip John Hardy; Kathy Hardy
Journal:  Transl Pediatr       Date:  2018-07
  8 in total

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