Literature DB >> 7327583

Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D.

H Rivera, C Turleau, J de Grouchy, C Junien, S Despoisse, J M Zucker.   

Abstract

Two cases of del(13)-retinoblastoma are reported. Case 1, a 13-month-old male, was monosomic due to the malsegregation of the maternal ins(20;13)(p12;q1307q14.3). The patients's sister was trisomic for 13q1307q14.3 with no evident phenotypic effect. Case 2 was a 20-month-old female with a denovo del(13)(q1303q14.3). In both instances esterase D activity showed a remarkable gene-dosage effect in monosomy, disomy, and trisomy, thus confirming the assignment of the gene locus to 13q14, and more precisely to the proximal half of this band. In all instances, the ESTD phenotypes were 1-1. It is suggested that esterase D activity should become an important diagnostic criteria for the various etiological forms of retinoblastoma.

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Year:  1981        PMID: 7327583     DOI: 10.1007/bf00283666

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


  9 in total

1.  Evidence for a null allele at the esterase D (EC 3.1.1.1) locus.

Authors:  R S Sparkes; S Targum; E Gershon; G F Sensabaugh; M C Sparkes; M Crist
Journal:  Hum Genet       Date:  1979-02-15       Impact factor: 4.132

2.  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

3.  Retinoblastoma, chromosome 13, and in vitro cellular radiosensitivity.

Authors:  J Nove; J B Little; R R Weichselbaum; W W Nichols; E Hoffman
Journal:  Cytogenet Cell Genet       Date:  1979

4.  Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14.

Authors:  R S Sparkes; M C Sparkes; M G Wilson; J W Towner; W Benedict; A L Murphree; J J Yunis
Journal:  Science       Date:  1980-05-30       Impact factor: 47.728

5.  Retinoblastoma and subband deletion of chromosome 13.

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

6.  [Retinoblastoma and interstitial deletion of 13q (author's transl)].

Authors:  J De Grouchy; C Turleau; M O Cabanis; J M Richardet
Journal:  Arch Fr Pediatr       Date:  1980-10

7.  [Increased sister-chromatid exchanges in fibroblasts from a del(13)-retinoblastoma patient (author's transl)].

Authors:  C Turleau; M O Cabanis; J de Grouchy
Journal:  Ann Genet       Date:  1980

8.  Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas.

Authors:  V M Riccardi; H M Hittner; U Francke; S Pippin; G P Holmquist; F L Kretzer; R Ferrell
Journal:  Clin Genet       Date:  1979-04       Impact factor: 4.438

Review 9.  Genetics of retinoblastoma.

Authors:  F Vogel
Journal:  Hum Genet       Date:  1979-11-01       Impact factor: 4.132

  9 in total
  17 in total

Review 1.  Chromosome imbalance, normal phenotype, and imprinting.

Authors:  L Bortotto; E Piovan; R Furlan; H Rivera; O Zuffardi
Journal:  J Med Genet       Date:  1990-09       Impact factor: 6.318

2.  Hereditary retinoblastoma: can balanced insertion entirely explain the differences of expressivity among families?

Authors:  C Bonaïti-Pellié; F Clerget-Darpoux; M C Babron
Journal:  Hum Genet       Date:  1990-12       Impact factor: 4.132

Review 3.  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

Review 4.  Microcytogenetics 1984.

Authors:  J de Grouchy; C Turleau
Journal:  Experientia       Date:  1986-10-15

5.  Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.

Authors:  W Cavenee; R Leach; T Mohandas; P Pearson; R White
Journal:  Am J Hum Genet       Date:  1984-01       Impact factor: 11.025

6.  The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation.

Authors:  F Rivas; H Rivera; M L Plascencia; B Ibarra; J M Cantú
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

Review 7.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

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

8.  The genetics of retinoblastoma, revisited.

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

9.  Familial retinoblastoma (mother and son) with 13q14 deletion.

Authors:  Y Fukushima; Y Kuroki; T Ito; I Kondo; I Nishigaki
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

10.  Low incidence of deletion of the esterase D locus in retinoblastoma patients.

Authors:  T P Dryja; G A Bruns; B Gallie; R Petersen; W Green; J M Rapaport; D M Albert; P S Gerald
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

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