Literature DB >> 7287000

Lymphocyte chromosome survey in 42 patients with retinoblastoma: effort to detect 13q14 deletion mosaicism.

T Motegi.   

Abstract

The results of a lymphocyte chromosome survey of retinoblastoma (Rb) patients using a method able to detect a relatively low proportion mosaicism of 13q14 deletion are presented. Three out of 42 Rb patients had abnormal karyotypes; two mosaic cases with the karyotype 46,XY,del(13) (q14.1q14.3)/46,XY and 46,XX,del(13)(q14.1q14.3)/46,XX (the proportions of 13q14-cells, 51% and 9%, respectively), and the other with the karyotype 46,XY,del(13)(q14.1q21.2). All of these three cases had bilateral sporadic Rb. Two mosaic cases had an apparently normal phenotype except for Rb. These data suggest that the frequency of Rb cases with a 13q- cell line in lymphocytes may be greater than that which has been reported.

Entities:  

Mesh:

Year:  1981        PMID: 7287000     DOI: 10.1007/BF00278704

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  25 in total

1.  Retinoblastoma and D-chromosome deletions.

Authors:  M G Wilson; J W Towner; A Fujimoto
Journal:  Am J Hum Genet       Date:  1973-01       Impact factor: 11.025

2.  Retinoblastoma and deletion D (14) syndrome.

Authors:  M G Wilson; J Melnyk; J W Towner
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

3.  Dq-, Dr and retinoblastoma.

Authors:  A I Taylor
Journal:  Humangenetik       Date:  1970

4.  Exclusion of chromosomal mosaicism: tables of 90%, 95% and 99% confidence limits and comments on use.

Authors:  E B Hook
Journal:  Am J Hum Genet       Date:  1977-01       Impact factor: 11.025

5.  Evolution of chromosomal abnormalities in sequential cytogenetic studies of ataxia telangiectasia.

Authors:  A Al Saadi; M Palutke; G K Kumar
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

6.  Absence of chromosome breakage in patients with retinoblastoma.

Authors:  L A Knight; H A Gardner; B L Gallie
Journal:  Hum Genet       Date:  1979-09-02       Impact factor: 4.132

7.  Sporadic bilateral retinoblastoma and 13q- chromosomal deletion.

Authors:  U Francke; F Kung
Journal:  Med Pediatr Oncol       Date:  1976

8.  Retinoblastoma. A model of hereditary fragile chromosomal regions.

Authors:  N Hashem; S Khalifa
Journal:  Hum Hered       Date:  1975       Impact factor: 0.444

9.  Retinoblastoma and subband deletion of chromosome 13.

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

10.  Retinoblastoma with 13q- chromosomal deletion associated with maternal paracentric inversion of 13q.

Authors:  R S Sparkes; H Muller; I Klisak
Journal:  Science       Date:  1979-03-09       Impact factor: 47.728

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  14 in total

1.  A genetic study of retinoblastoma.

Authors:  X X Liu; Y J Sun; L Zhang
Journal:  J Tongji Med Univ       Date:  1991

2.  Patients with retinoblastoma and chromosome 13q deletions have increased chemotherapy-related toxicities.

Authors:  Rachel C Brennan; Ibrahim Qaddoumi; Catherine A Billups; Tracy Kaluzny; Wayne L Furman; Matthew W Wilson
Journal:  Pediatr Blood Cancer       Date:  2016-07-13       Impact factor: 3.167

3.  Is the interstitial deletion of 13q in retinoblastoma patients not transmissible?

Authors:  T Motegi; M Komatsu; K Minoda
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods).

Authors:  T Motegi
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

5.  The genetics of retinoblastoma, revisited.

Authors:  A Naumova; C Sapienza
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

6.  A decreasing tendency for cytogenetic abnormality in peripheral lymphocytes of retinoblastoma patients with 13q14 deletion mosaicism.

Authors:  T Motegi; K Minoda
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Retinoblastoma in a boy with a de novo mutation of a 13/18 translocation: the assumption that the retinoblastoma locus is at 13q141, particularly at the distal portion of it.

Authors:  T Motegi; M Komatsu; Y Nakazato; M Ohuchi; K Minoda
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

8.  Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study.

Authors:  V R Babu; D L Van Dyke; C E Jackson
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

9.  A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13q.

Authors:  T Motegi; M Kaga; Y Yanagawa; H Kadowaki; K Watanabe; A Inoue; M Komatsu; K Minoda
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

10.  Bilateral retinoblastoma with de novo constitutional balanced translocation t(2;9)(q11;p11).

Authors:  P Balestrazzi; M G Mattei; M A Baeteman; J F Mattei; F Giraud
Journal:  Eur J Pediatr       Date:  1984-02       Impact factor: 3.183

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