Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12-Reference-Cited by-同舟云学术

Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12

Published:2007-11-14 Issue:1 Volume:73 Page:44-49
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Davidsson J,Collin A,Öreberg M,Gisselsson D

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00917.x/fullpdf

Reference24 articles.

1. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics;Liehr;Int J Mol Med,2007

2. Small supernumerary marker chromosomes-progress towards a genotype-phenotype correlation;Liehr;Cytogenet Genome Res,2006

3. Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization;Blennow;Prenat Diagn,1994

4. Small extra ring chromosome derived from chromosome 10p: clinical report and characterisation by FISH;Blennow;J Med Genet,1996

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the mother;European Journal of Paediatric Neurology;2011-05

2. Contribution of array CGH in prognosis and genetic counselling of prenatally diagnosed supernumerary ring chromosome 20;Prenatal Diagnosis;2009-08-10

3. Mosaic ring chromosome 8: Clinical and array-CGH findings in partial trisomy 8;American Journal of Medical Genetics Part A;2008-11-01