MLPA: A prenatal diagnostic tool for the study of congenital heart defects?-Reference-Cited by-同舟云学术

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MLPA: A prenatal diagnostic tool for the study of congenital heart defects?

Published:2012-05 Issue:1 Volume:500 Page:151-154
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Mademont-Soler Irene,Morales Carme,Soler Anna,Clusellas Núria,Margarit Ester,Martínez-Barrios Estefanía,Martínez José María,Sánchez Aurora

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference21 articles.

1. Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis;Armengol;Hum. Genet.,2011

2. Investigating 22q11.2 deletion and other chromosomal aberrations in fetuses with heart defects detected by prenatal echocardiography;Bellucco;Pediatr. Cardiol.,2010

3. Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects;Breckpot;J. Pediatr.,2010

4. Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome;Bretelle;Eur. J. Med. Genet.,2010

5. Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype;D'Amours;Clin. Genet.,2012

Cited by 11 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. Conotruncal Heart Defects: A Narrative Review of Molecular Genetics, Genomics Research and Innovation;OMICS: A Journal of Integrative Biology;2024-07-01

2. 22q11 Copy Number Variations in a Brazilian Cohort of Children with Congenital Heart Disorders;Molecular Syndromology;2022-07-04

3. MLPA analysis of 32 foetuses with a congenital heart defect and 1 foetus with renal defects - pilot study. The significant frequency rate of presented pathological CNV;Biomedical Papers;2021-03-31

4. Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect;Molecular Cytogenetics;2015-12

5. The First Case Report in Italy of Di George Syndrome Detected by Noninvasive Prenatal Testing;Case Reports in Obstetrics and Gynecology;2015

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