Literature DB >> 7205909

13q-/r(13) mosaicism.

N Niikawa, T Tamura, F Tomiyasu, T Kajii.   

Abstract

A 2-month-old female infant with typical features of the 13q-syndrome was found to be a hitherto unreported mosaic consisting of 46,XX,del(13)(q22)-46,XX,r(13)(p13q22). Both of the 13q- and r(13) chromosomes were Ag N banding positive. Therefore, it was assumed that they had retained the satellite stalks. Two possible mechanisms were proposed for the genesis of the mosaicism. Firstly, the patients started with the 13q- chromosome, which then underwent breakage and reunion at both ends to form the r(13) chromosome. Secondly, the patients started with the r(13) chromosome, which reopened at or close to the joining point to form the 13q- chromosome.

Entities:  

Mesh:

Year:  1980        PMID: 7205909      PMCID: PMC1048579          DOI: 10.1136/jmg.17.4.316

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


  7 in total

1.  Familial short arm deletion of chromosome no. 15.

Authors:  J J Hoo; U Hillig; H Cramer; S Hansen; F Hermann
Journal:  Humangenetik       Date:  1974

2.  Frequency of deletion of short arm satellites in acrocentric chromosomes.

Authors:  J Nielsen; U Friedrich; A B Hreidarsson
Journal:  J Med Genet       Date:  1974-06       Impact factor: 6.318

3.  Human chromosome abnormalities revisited.

Authors:  M W Shaw
Journal:  Am J Hum Genet       Date:  1972-03       Impact factor: 11.025

4.  An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes.

Authors:  S E Bloom; C Goodpasture
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

5.  Retinoblastoma and subband deletion of chromosome 13.

Authors:  J J Yunis; N Ramsay
Journal:  Am J Dis Child       Date:  1978-02

6.  Partial deletions and trisomies of chromosome 13; mapping of bands associated with particular malformations.

Authors:  B Noel; B Quack; M O Rethore
Journal:  Clin Genet       Date:  1976-06       Impact factor: 4.438

7.  Ring chromosome 13 in a child with minor dysmorphic features. Irregular phenotypic expression of ring 13 syndrome.

Authors:  R S Verma; H Dosik; I H Chowdhry; R C Jhaveri
Journal:  Am J Dis Child       Date:  1978-10
  7 in total
  2 in total

1.  High-resolution cytogenetic characterization of telomeric associations in ring chromosome 19.

Authors:  J R Sawyer; R A Rowe; S J Hassed; C Cunniff
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

Review 2.  Distribution of break points in human structural rearrangements.

Authors:  Y Nakagome; T Matsubara; H Fujita
Journal:  Am J Hum Genet       Date:  1983-03       Impact factor: 11.025

  2 in total

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