Literature DB >> 7069753

A severely retarded male with deletion of chromosomes 15 (pter leads to q13) and 10 (q 26 leads to qter).

A Smith, G den Dulk.   

Abstract

Entities:  

Mesh：

Year:  1982        PMID： 7069753      PMCID： PMC1048826          DOI： 10.1136/jmg.19.1.77

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


× No keyword cloud information.
  1 in total

1.  Mental retardation associated with "balanced" chromosome rearrangements.

Authors:  S J Funderburk; M A Spence; R S Sparkes
Journal:  Am J Hum Genet       Date:  1977-03       Impact factor: 11.025
  1 in total
  4 in total

1.  Investigations with fluorescence in situ hybridization (FISH) demonstrate loss of the telomeres on the reciprocal chromosome in three unbalanced translocations involving chromosome 15 in the Prader-Willi and Angelman syndromes.

Authors:  A Jauch; L Robson; A Smith
Journal:  Hum Genet       Date:  1995-09       Impact factor: 4.132

Review 2.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

3.  Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases.

Authors:  J F Mattei; M G Mattei; F Giraud
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Unbalanced reciprocal translocations in cases of Prader-Willi syndrome.

Authors:  D P Duckett; S H Roberts; P Davies
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.