Literature DB >> 5474810

A complex familial translocation involving chromosomes 5, 9 and 13.

K Fredga, B Hall.   

Abstract

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Year:  1970        PMID： 5474810     DOI： 10.1159/000130099

Source DB:  PubMed          Journal:  Cytogenetics        ISSN： 0011-4537


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  7 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.  Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement.

Authors:  M H Bogart; C L Bradshaw; O W Jones; J E Schanberger
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318

3.  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

4.  Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome.

Authors:  H Fujita; T Abe; K Yamamoto; J Furuyama
Journal:  Humangenetik       Date:  1974

5.  A familial reciprocal translocation between three chromosomes.

Authors:  M R Creasy; J A Crolla; M G Daker
Journal:  Humangenetik       Date:  1974

6.  A complex rearrangement involving three autosomes in a phenotypically normal male presenting with sterility.

Authors:  A Joseph; I M Thomas
Journal:  J Med Genet       Date:  1982-10       Impact factor: 6.318

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
  7 in total

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