Prenatal Diagnosis of Merosin-Deficient Muscular Dystrophy-Reference-Cited by-同舟云学术

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Prenatal Diagnosis of Merosin-Deficient Muscular Dystrophy

Published:2018-10-25 Issue:6 Volume:37 Page:418-423
ISSN:1551-3815
Container-title:Fetal and Pediatric Pathology
language:en
Short-container-title:Fetal and Pediatric Pathology

Author:

Fadiloglu Erdem¹^ORCID,Ozten Gonca¹,Unal Canan¹,Talim Beril²,Topaloglu Haluk³,Beksac Mehmet Sinan¹

Affiliation:

1. Division of Perinatology, Department of Obstetrics and Gynecology, Ankara, Turkey;

2. Division of Pediatric Pathology, Department of Pediatrics, Ankara, Turkey;

3. Division of Pediatric Neurology, Department of Pediatrics, Hacettepe University Medical Faculty, Ankara, Turkey

Publisher

Informa UK Limited

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/15513815.2018.1520944

Reference21 articles.

1. Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy

2. Structure of the Human Laminin α2-Chain Gene (LAMA2), Which Is Affected in Congenital Muscular Dystrophy

3. Merosin-deficient congenital muscular dystrophy: A novel homozygous mutation in the laminin-2 gene

4. Prenatal diagnosis in laminin α2 chain (merosin)-deficient congenital muscular dystrophy: A collective experience of five international centers

5. Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients

Cited by 4 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. Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients;Frontiers in Genetics;2023-06-14

2. Utility of immunohistochemistry and western blot in profiling clinically suspected cases of congenital muscular dystrophy;Annals of Indian Academy of Neurology;2021

3. A Novel Frameshift Mutation in Two Siblings with Merosin-deficient Congenital Muscular Dystrophy;Medical Bulletin of Haseki;2020-03-01

4. Chorionic villus sampling experience of a reference perinatal medicine center;Annals of Human Genetics;2019-12-04

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