Preimplantation genetic diagnosis for myotonic dystrophy type 1: detection of crossover between the gene and the linked marker APOC2-Reference-Cited by-同舟云学术

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Preimplantation genetic diagnosis for myotonic dystrophy type 1: detection of crossover between the gene and the linked marker APOC2

Published:2007 Issue:2 Volume:27 Page:111-116
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Kakourou Georgia,Dhanjal Seema,Daphnis Danny,Doshi Alpesh,Nuttall Sarah,Gotts Sarah,Serhal Paul,Delhanty Joy,Harper Joyce,SenGupta Sioban

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference18 articles.

1. Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy

2. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

3. The contribution of cis-elements to disease-associated repeat instability: clinical and experimental evidence

4. Intergenerational Instability of the Expanded CTG Repeat in the DMPK Gene: Studies in Human Gametes and Preimplantation Embryos

5. Paternal transmission of congenital myotonic dystrophy.

Cited by 24 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. Preimplantation genetic testing for embryos predisposed to hereditary cancer: Possibilities and challenges;Cancer Pathogenesis and Therapy;2024-01

2. A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran;BMC Pregnancy and Childbirth;2022-04-15

3. A novel method for noninvasive diagnosis of monogenic diseases from circulating fetal cells;Prenatal Diagnosis;2020-11-04

4. The impact of parental unaffected allele combination on the diagnostic outcome in the preimplantation genetic testing for myotonic dystrophy type 1 in Japanese ancestry;Reproductive Medicine and Biology;2020-04-29

5. Robust Preimplantation Genetic Testing Strategy for Myotonic Dystrophy Type 1 by Bidirectional Triplet-Primed Polymerase Chain Reaction Combined With Multi-microsatellite Haplotyping Following Whole-Genome Amplification;Frontiers in Genetics;2019-06-26

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