Literature DB >> 626181

Retinoblastoma and subband deletion of chromosome 13.

J J Yunis, N Ramsay.   

Abstract

Two patients with retinoblastoma and an interstitial deletion of the long arm of chromosome 13 were studied using G-banded metaphase and prophase chromosomes. One patient showed several congenital defects, developmental retardation, and deletion of bands q14 and q21. The second patient showed mild developmental delay, a few minor congenital defects, and a loss of approximately half of band q14. On the basis of this study and nine others from the literature, it is now possible to tentatively assign a predisposition to retinoblastoma to deletion of a specific small region of chromosome 13.

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Year:  1978        PMID: 626181     DOI: 10.1001/archpedi.1978.02120270059012

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  92 in total

Review 1.  Molecular genetic abnormalities in the pathogenesis of human lung cancer.

Authors:  E Forgacs; S Zöchbauer-Müller; E Oláh; J D Minna
Journal:  Pathol Oncol Res       Date:  2001       Impact factor: 3.201

2.  [Comparative genomic hybridization as cytogenetic tumor diagnosis technique in juvenile angiofibroma].

Authors:  H Löwenheim
Journal:  HNO       Date:  2003-12       Impact factor: 1.284

Review 3.  Tumor suppressor genes: a new era for molecular genetic studies of cancer.

Authors:  E Y Lee
Journal:  Breast Cancer Res Treat       Date:  1991-09       Impact factor: 4.872

4.  Y/6 chromosome translocation in a male with triple primary cancers involving the breast.

Authors:  A Kojima; T Ikeuchi; M Inomata; T Shinkai; K Ishihara; M Noguchi; N Saijo
Journal:  J Cancer Res Clin Oncol       Date:  1991       Impact factor: 4.553

5.  Construction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map.

Authors:  M J Higgins; C Turmel; J Noolandi; P E Neumann; M Lalande
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

6.  Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.

Authors:  P J Goodfellow; B N White; J J Holden; A M Duncan; E V Sears; H S Wang; L Berlin; K K Kidd; N E Simpson
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

7.  Family studies on the chromosomal location of the retinoblastoma gene (Rb-1).

Authors:  J Morten; D G Harnden; S Bundey
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318

8.  A detailed analysis of chromosomal changes in heritable and non-heritable retinoblastoma.

Authors:  J Squire; B L Gallie; R A Phillips
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

9.  18q-syndrome and extraskeletal Ewing's sarcoma.

Authors:  M Machin Valtueña; J M Garcia-Sagredo; A Muñoz Villa; C Lozano Giménez; J M Aparicio Meix
Journal:  J Med Genet       Date:  1987-07       Impact factor: 6.318

10.  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

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