Literature DB >> 730167

[A case of bilateral retinoblastoma with monosomy 13 (q12 leads to 114) (author's transl)].

R Walbaum, P François, J P Farriaux, M Woillez.   

Abstract

A partial monosomy 13 by interstitial deletion was found in the complement of a girl with mild mental retardation and bilateral retinoblastoma. Break points were at 13q12 and 13q14. After comparison with other known observations of retinoblastoma with deletion of chromosome 13, it is suggested that the deletion common to these patients may be band 13q14. The most likely pathogenic hypothesis seems to be the haplo-insufficiency.

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Year:  1978        PMID: 730167     DOI: 10.1007/bf00295418

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


  24 in total

1.  A case of Down's syndrome complicated by retinoblastoma and celiac disease.

Authors:  D Bentley
Journal:  Pediatrics       Date:  1975-07       Impact factor: 7.124

2.  ASSOCIATION OF RETINOBLASTOMA WITH MENTAL DEFECT AND OTHER PATHOLOGICAL MANIFESTATIONS.

Authors:  A TAKTIKOS
Journal:  Br J Ophthalmol       Date:  1964-09       Impact factor: 4.638

3.  Retinoblastoma and chromosome 13.

Authors:  U Francke
Journal:  Cytogenet Cell Genet       Date:  1976

4.  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

5.  The 13q- deletion syndrome.

Authors:  E Grace; J Drennan; D Colver; R R Gordon
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318

6.  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

7.  Retinoblastoma: epidemiologic characteristics.

Authors:  R D Jensen; R W Miller
Journal:  N Engl J Med       Date:  1971-08-05       Impact factor: 91.245

8.  Chromosomal analysis of a human retinoblastoma.

Authors:  J Mark
Journal:  Acta Ophthalmol (Copenh)       Date:  1970

9.  Dq-, Dr and retinoblastoma.

Authors:  A I Taylor
Journal:  Humangenetik       Date:  1970

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

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

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  6 in total

1.  Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis.

Authors:  K Mangelschots; B Van Roy; F Speleman; N Van Roy; J Gheuens; J Beuten; I Buntinx; M N Van Thienen; H Willekens; J Dumon
Journal:  Hum Genet       Date:  1992-06       Impact factor: 4.132

Review 2.  13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature review.

Authors:  Gregory Costain; Candice K Silversides; Christian R Marshall; Mary Shago; Nicholas Costain; Anne S Bassett
Journal:  Int J Cardiol       Date:  2010-07-03       Impact factor: 4.164

3.  Retinoblastoma, gross internal malformations, and deletion 13q14 leads to q31.

Authors:  E Yunis; R Zuñiga; E Ramírez
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  Retinoblastoma: host resistance and 13q- chromosomal deletion.

Authors:  E Matsunaga
Journal:  Hum Genet       Date:  1980       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.  Interstitial deletion 13q syndromes: a report on two unrelated patients.

Authors:  M Serena-Lungarotti; A Calabro; G Mariotti; P P Mastroiacovo; S Provenzano; B Dallapiccola
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

  6 in total

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