Noninvasive prenatal diagnosis of Huntington disease: detection of the paternally inherited expanded CAG repeat in maternal plasma

Author:

van den Oever Jessica M. E.1,Bijlsma Emilia K.1,Feenstra Ilse2,Muntjewerff Nienke3,Mathijssen Inge B.4,Bakker Egbert1,van Belzen Martine J.1,Boon Elles M. J.1

Affiliation:

1. Department of Clinical Genetics; Leiden University Medical Center; Leiden The Netherlands

2. Department of Human Genetics; Radboud University Medical Center; Nijmegen The Netherlands

3. Department of Clinical Genetics; Maastricht University Medical Center; Maastricht The Netherlands

4. Department of Clinical Genetics; Academic Medical Center; Amsterdam The Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference21 articles.

1. Huntingtin and the molecular pathogenesis of Huntington's disease. Fourth in molecular medicine review series;Landles;EMBO Rep,2004 Oct

2. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group;The Huntington's Disease Collaborative Research Group;Cell,1993 Mar 26

3. Unstable familial transmissions of Huntington disease alleles with 27-35 CAG repeats (intermediate alleles);Semaka;Am J Med Genet B Neuropsychiatr Genet,2010 Jan 5

4. Reproductive options for prospective parents in families with Huntington's disease: clinical, psychological and ethical reflections;Die-Smulders;Hum Reprod Update,2013 May

5. Comparison of chorionic villus sampling and amniocentesis for fetal karyotyping at 10-13 weeks' gestation;Nicolaides;Lancet,1994 Aug 13

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