Literature DB >> 6725007

Partial trisomy 15(q25qter) in two brothers.

U Kristoffersson, B Bergwall.   

Abstract

Entities:  

Mesh：

Year:  1984        PMID： 6725007     DOI： 10.1111/j.1601-5223.1984.tb00097.x

Source DB:  PubMed          Journal:  Hereditas        ISSN： 0018-0661            Impact factor:   3.271


× No keyword cloud information.
  4 in total

1.  Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.

Authors:  D Wieczorek; H Engels; R Viersbach; B Henke; G Schwanitz; E Passarge
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

2.  Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.

Authors:  E Blennow; H Telenius; D de Vos; C Larsson; P Henriksson; O Johansson; N P Carter; M Nordenskjöld
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

3.  Partial trisomy of chromosome 15q and partial monopsony of 6q due to maternal balanced translocation.

Authors:  Shilpy Singla; Kausik Mandal; Suvasini Sharma; Viswas Chhapola
Journal:  J Pediatr Neurosci       Date:  2014-05

4.  Chromosome 15 structural abnormalities: effect on IGF1R gene expression and function.

Authors:  Rossella Cannarella; Teresa Mattina; Rosita A Condorelli; Laura M Mongioì; Giuseppe Pandini; Sandro La Vignera; Aldo E Calogero
Journal:  Endocr Connect       Date:  2017-10       Impact factor: 3.335
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.