Literature DB >> 304698

Familial partial trisomy 15.

M M Power, R G Barry, D E Cannon, J G Masterson.   

Abstract

A family, including two sibs with partial trisomy 15 is described. Maternal chromosome analysis revealed 46,XX/47,XX,+15q-, mosaicism. These findings are discussed in relation to seventeen previously published cases, some of which were sporadic and others due to maternal balanced translocation.

Mesh：

Year:  1977        PMID： 304698

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  5 in total

1.  A new case of partial trisomy 15q-.

Authors:  A Geneix; J Y Jaffray; P Malet; E Foulon; P Jalbert; P Crost
Journal:  Hum Genet       Date:  1979-10-02       Impact factor: 4.132

2.  De novo partial trisomy 15q (proximal type).

Authors:  T J Herweijer; J W Oorthuys; N J Leschot
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

3.  The genetic significance of accessory bisatellited marker chromosomes.

Authors:  P Steinbach; M Djalali; I Hansmann; E Kattner; M Meisel-Stosiek; H D Probeck; A Schmidt; M Wolf
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Cytogenetic and clinical studies in five cases of inv dup(15).

Authors:  L Wisniewski; T Hassold; J Heffelfinger; J V Higgins
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

Review 5.  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
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.