Literature DB >> 4544095

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

J Martinetti, B Noel.   

Abstract

Entities:  

Mesh：

Year:  1973        PMID： 4544095

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


× No keyword cloud information.
  6 in total

1.  Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20.

Authors:  C G Palmer; C Poland; T Reed; J Kojetin
Journal:  Hum Genet       Date:  1976-02-29       Impact factor: 4.132

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

Authors:  S Walker; P J Howard; D Hunter
Journal:  J Med Genet       Date:  1985-12       Impact factor: 6.318

3.  Segregation of a complex rearrangement of chromosomes 6, 7, 8, and 12 through three generations.

Authors:  B Meer; G Wolff; E Back
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  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

5.  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

6.  A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.

Authors:  G Simoni; E Montali; F Rossella; L Dalprà; F Lo Curto
Journal:  Hum Genet       Date:  1979-01-25       Impact factor: 4.132
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.