Literature DB >> 991443

Structural aberrations of the long arm of chromosome no. 22. Report fo a family with translocation t(11;22) (q25;q11).

W Fu, D S Borgaonkar, P P Ladewig, J Weaver, H H Pomerance.   

Abstract

A chromosomal translocation t(11;22) (q25q11) is described in a family. Four members, in two generations, had the same translocation but showed phenotypic variation. Case reports of chromosome aberrations involving the long arm of chromosome 22 associated with and without chronic myeloid leukemia (CML) are reviewed. It appears that the distal segment of the long arm or chromosome 22 is either translocated or deleted, resulting in congenital anomalies, presumably due to chromosome imbalance. In other instances, a specific breakpoint on 22q results in the origin of Philadelphia chromosome (Ph1) associated with CML.

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Year:  1976        PMID: 991443     DOI: 10.1111/j.1399-0004.1976.tb00057.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  9 in total

1.  A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).

Authors:  Molly B Sheridan; Takema Kato; Chad Haldeman-Englert; G Reza Jalali; Jeff M Milunsky; Ying Zou; Ruediger Klaes; Georgio Gimelli; Stefania Gimelli; Robert M Gemmill; Harry A Drabkin; April M Hacker; Julia Brown; David Tomkins; Tamim H Shaikh; Hiroki Kurahashi; Elaine H Zackai; Beverly S Emanuel
Journal:  Am J Hum Genet       Date:  2010-07-30       Impact factor: 11.025

2.  Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.

Authors:  C Carlson; H Sirotkin; R Pandita; R Goldberg; J McKie; R Wadey; S R Patanjali; S M Weissman; K Anyane-Yeboa; D Warburton; P Scambler; R Shprintzen; R Kucherlapati; B E Morrow
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

3.  Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

Authors:  J C Barber; C A Joyce; M N Collinson; J C Nicholson; L R Willatt; H M Dyson; M S Bateman; A J Green; J R Yates; N R Dennis
Journal:  J Med Genet       Date:  1998-06       Impact factor: 6.318

4.  Deletion mapping of 22q11 in CATCH22 syndrome: identification of a second critical region.

Authors:  H Kurahashi; T Nakayama; Y Osugi; E Tsuda; M Masuno; K Imaizumi; T Kamiya; T Sano; S Okada; I Nishisho
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

5.  Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis.

Authors:  D H Lockwood; A Farrier; F Hecht; J Allanson
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

Review 6.  Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.

Authors:  P Jalbert; B Sele
Journal:  J Med Genet       Date:  1979-12       Impact factor: 6.318

7.  The 11q;22q translocation: a European collaborative analysis of 43 cases.

Authors:  M Fraccaro; J Lindsten; C E Ford; L Iselius
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

Review 8.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

9.  Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183).

Authors:  M P Mulder; M Wilke; A Langeveld; L G Wilming; A Hagemeijer; E van Drunen; E C Zwarthoff; P H Riegman; W H Deelen; A M van den Ouweland
Journal:  Hum Genet       Date:  1995-08       Impact factor: 4.132

  9 in total

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