Literature DB >> 891004

Chromosomal anomalies in patients with retinoblastoma.

M G Wilson, A J Ebbin, J W Towner, W H Spencer.   

Abstract

Karyotypes from 50 persons with retinoblastoma confirmed by histopathological examination were studied by conventional staining and Giemsa-banding techniques. Two chromosomal anomalies were found. An interstitial deletion of the long arm of No. 13 chromosome was identified by Giemsa-banding in the karyotypes from a boy with unilateral retinoblastoma. Another boy with unilateral tumor had a karyotype of 47,XXY. These findings provide additional evidence that a deletion of chromosome No. 13, most likely involving band 13q14, is associated with the development of retinoblastoma. In conjunction with other reports, our findings also suggest that retinoblastoma may be found more frequently in children with chromosomal aneuploidy.

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Year:  1977        PMID: 891004     DOI: 10.1111/j.1399-0004.1977.tb00894.x

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


  23 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

Review 3.  Genetics of neoplasia--impact of ecogenetics on oncogenesis. A review.

Authors:  D T Purtilo; L Paquin; T Gindhart
Journal:  Am J Pathol       Date:  1978-06       Impact factor: 4.307

4.  Interstitial deletion of chromosome 13 and associated congenital anomalies.

Authors:  W W Nichols; R C Miller; E Hoffman; D Albert; R R Weichselbaum; J Nove; J B Little
Journal:  Hum Genet       Date:  1979-11       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

7.  Monocyte esterase deficiency in malignant neoplasia.

Authors:  G M Markey; J A McCormick; T C Morris; H D Alexander; L Nolan; L M Morgan; M E Reynolds; S Edgar; A L Bell; M D McCaigue
Journal:  J Clin Pathol       Date:  1990-04       Impact factor: 3.411

8.  Multiple endocrine neoplasia type 2 (Sipple's syndrome): clinical and cytogenetic analysis of a kindred.

Authors:  A Zatterale; M Stabile; V Nunziata; G Di Giovanni; R Vecchione; V Ventruto
Journal:  J Med Genet       Date:  1984-04       Impact factor: 6.318

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

Authors:  R Walbaum; P François; J P Farriaux; M Woillez
Journal:  Hum Genet       Date:  1978-10-31       Impact factor: 4.132

10.  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

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