Literature DB >> 3841161

Familial complex autosomal translocations involving chromosomes 7, 8, and 9 exhibiting male and female transmission with segregation and recombination.

S Walker, P J Howard, D Hunter.   

Abstract

A family showing a complex translocation between chromosomes 7, 8, and 9 with breakpoints at 7q21, 7q33, 8p23, and 9p23 is described. The proband had been referred because of repeated spontaneous abortions. This is only the second family to be ascertained in this way. Twenty-three other cases of complex translocations are briefly reviewed, eight of which were de novo in origin and 15 familial. All but one of the familial cases showed maternal transmission only. The present family shows both maternal and paternal transmission and is thought to be the first exhibiting recombination from a male carrier. The origin and transmission of the complex translocation is followed through three generations.

Mesh：

Year:  1985        PMID： 3841161      PMCID： PMC1049510          DOI： 10.1136/jmg.22.6.484

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


  23 in total

1.  [Complexe de novo rearrangement involving 4 chromosomes in a newborn infant].

Authors:  J Martinetti; B Noel
Journal:  Ann Genet       Date:  1973-12

2.  [Partial trisomies of the long arm of 7 chromosome].

Authors:  R Berger; J Derre; M A Ortiz
Journal:  Nouv Presse Med       Date:  1974-09-07

3.  Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.

Authors:  O Sanchez; J J Yunis; J I Escobar
Journal:  Humangenetik       Date:  1974-04-24

4.  Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.

Authors:  P W Allderdice; O J Miller; D A Miller; W R Breg; E Gendel; C Zelson
Journal:  Humangenetik       Date:  1971

5.  Complex balanced translocation of chromosomes 2, 3, and 13.

Authors:  R S Muneer; D L Donaldson; O M Rennert
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  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

7.  A complex double translocation involving four chromosomes and five breakpoints in a child with mild mental retardation.

Authors:  D A Couzin; J L Watt; I A Auchterlonie
Journal:  J Med Genet       Date:  1983-10       Impact factor: 6.318

8.  A complex rearrangement, including a deleted 8q, in a case of Langer-Giedion syndrome.

Authors:  S Schwartz; J H Beisel; S R Panny; M M Cohen
Journal:  Clin Genet       Date:  1985-02       Impact factor: 4.438

9.  A complex balanced rearrangement involving four chromosomes in an azoospermic man.

Authors:  M T Rodriguez; M J Martin; J A Abrisqueta
Journal:  J Med Genet       Date:  1985-02       Impact factor: 6.318

10.  A family with three independent autosomal translocations associated with 7q32----7qter syndrome.

Authors:  H N Bass; R S Sparkes; M M Lessner; M Fox; B Phoenix; J Bernar
Journal:  J Med Genet       Date:  1985-02       Impact factor: 6.318
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  5 in total

1.  De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma.

Authors:  E Calzolari; P Palazzi; V Aiello; E Mazzeo; P Perri; A Minelli; L del Senno; P Patracchini; F Bernardi
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

2.  Complex chromosomal rearrangement involving chromosomes 1, 4 and 22 in an infertile male: case report and literature review.

Authors:  I Salahshourifar; N Shahrokhshahi; T Tavakolzadeh; Z Beheshti; H Gourabi
Journal:  J Appl Genet       Date:  2009       Impact factor: 3.240

3.  De novo complex chromosomal rearrangement in a woman with recurrent spontaneous abortion and one healthy daughter.

Authors:  L Timár; J Béres; G Kosztolányi; I Németh
Journal:  Hum Genet       Date:  1991-02       Impact factor: 4.132

4.  Familial Infertility (Azoospermia and Cryptozoospermia) in Two Brothers-Carriers of t(1;7) Complex Chromosomal Rearrangement (CCR):  Molecular Cytogenetic Analysis.

Authors:  Marta Olszewska; Tomasz Stokowy; Nijole Pollock; Nataliya Huleyuk; Andrew Georgiadis; Svetlana Yatsenko; Danuta Zastavna; Alexander N Yatsenko; Maciej Kurpisz
Journal:  Int J Mol Sci       Date:  2020-06-26       Impact factor: 5.923

5.  7q36 deletion and 9p22 duplication: effects of a double imbalance.

Authors:  Karla de Oliveira Pelegrino; Sofia Sugayama; Ana Lúcia Catelani; Karina Lezirovitz; Fernando Kok; Maria de Lourdes Chauffaille
Journal:  Mol Cytogenet       Date:  2013-01-15       Impact factor: 2.009
  5 in total

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