Literature DB >> 145313

Report of large kinship with familial translocation between chromosomes 21 and 22.

J E Brissenden, M T Costa, M H Roberts.   

Abstract

This paper reports a large kinship with a familial (21;22) translocation occurring in both the balanced and the unbalanced states. Recurrence risks for the (21;22) translocation in the unbalanced state are high (14%) for the offspring of female carriers as compared with those for the offspring of male carriers (4%), but the offspring of male carriers appear to have a much higher risk (50%) of being balanced carriers than those of female carriers (30%).

Mesh:

Year:  1977        PMID: 145313      PMCID: PMC1880414     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN: 0008-4409            Impact factor:   8.262


  8 in total

1.  Familial C-G translocation causing mitotic nondisjunction. A cause of familial mosaic Down's syndrome.

Authors:  L Weiss; C B Wolf
Journal:  Am J Dis Child       Date:  1968-12

2.  Diverse chromosomal anomalies in a family.

Authors:  L Atkins; C S Bartsocas; P J Porter
Journal:  J Med Genet       Date:  1968-12       Impact factor: 6.318

3.  Robertsonian translocations in man: evidence for prezygotic selection.

Authors:  J L Hamerton
Journal:  Cytogenetics       Date:  1968

4.  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

5.  Spontaneous D-G translocation in fibroblasts derived from a patient with trisomy 21 mosaicism.

Authors:  G Kohn; M Aronson; W J Mellman
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

6.  Segregation analysis of a large t(21q22q) family.

Authors:  C J Chapman; R J Gardner; A M Veale
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318

7.  A statistical segregation analysis of (21q22q)-translocations.

Authors:  J Stene
Journal:  Hum Hered       Date:  1970       Impact factor: 0.444

8.  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

  8 in total

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