Prenatal diagnosis for CF using High Resolution Melting Analysis and simultaneous haplotype analysis through QF-PCR
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Reference12 articles.
1. Cystic fibrosis: a worldwide analysis of CFTR mutations–correlation with incidence data and application to screening;Bobadilla;Hum Mutat,2002
2. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA;Riordan;Science,1989
3. Comprehensive description of CFTR genotypes and ultrasound patterns in 694 cases of fetal bowel anomalies: a revised strategy;de Becdelievre;Hum Genet,2011
4. Cystic fibrosis genetic counseling difficulties due to the identification of novel mutations in the CFTR gene;Poulou;J Cyst Fibros,2012
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1. CFTR gene mutation spectrum among 735 Iranian patients with cystic fibrosis: A comprehensive systematic review;Pediatric Pulmonology;2021-09-15
2. Prenatal diagnosis of genetic diseases directly using paper-dried cord blood as the starting material for PCR;Analytical and Bioanalytical Chemistry;2019-08-13
3. High Resolution Melting (HRM) for High-Throughput Genotyping—Limitations and Caveats in Practical Case Studies;International Journal of Molecular Sciences;2017-11-03
4. Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD);Journal of Cystic Fibrosis;2016-03
5. Complex preimplantation genetic diagnosis for beta-thalassaemia, sideroblastic anaemia, and human leukocyte antigen (HLA)-typing;Systems Biology in Reproductive Medicine;2015-12-04
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