Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of β-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS cases-Reference-Cited by-同舟云学术

Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of β-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS cases

Published:2019-05-15 Issue:1 Volume:9 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Sharifi Zohreh,Rahiminejad Faezeh,Joudaki Atefeh,Bandehi Ameneh Sarhadi,Farahzadi Hossein,Keshvar Yeganeh,Golnabi Fatemeh,Naderi Sanaz,Yazdani Rasaneh,Shafaat Mehdi,Ghadami Shirin,Abiri Maryam,Zeinali Sirous

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-019-43892-2.pdf

Reference42 articles.

1. Galanello, R. & Origa, R. Beta-thalassemia. J. Orphanet journal of rare diseases. 5, 11, https://doi.org/10.1186/1750-1172-5-11 (2010).

2. Rathod, D. A. et al. Usefulness of cell counter–based parameters and formulas in detection of β-thalassemia trait in areas of high prevalence. J. American Journal of Clinical Pathology. 128, 585–589 (2007).

3. Hossain, M. S. et al. Thalassemias in South Asia: clinical lessons learnt from Bangladesh. J. Orphanet journal of rare diseases. 12, 93 (2017).

4. Abolghasemi, H. et al. Thalassemia in Iran: epidemiology, prevention, and management. J. Pediatric Hematology/Oncology. 29, 233–238 (2007).

5. Fallah, M. S., Samavat, A. & Zeinali, S. Iranian national program for the prevention of thalassemia and prenatal diagnosis: mandatory premarital screening and legal medical abortion. J. Prenatal Diagnosis. 29, 1285–1286 (2009).

Cited by 6 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. Asian Screening Array and Next‐Generation Sequencing Based Panels Applied to Preimplantation Genetic Testing for Monogenic Disorders Preclinical Workup in 294 Families: A Retrospective Analysis;Prenatal Diagnosis;2024-07-27

2. Comprehensive application of multiple molecular diagnostic techniques in pre‐implantation genetic testing for monogenic;Molecular Genetics & Genomic Medicine;2023-10-12

3. Prenatal Diagnosis: The Main Advances in the Application of Identification of Biomarkers Based on Multi-Omics;Ectopic Pregnancy and Prenatal Diagnosis;2022-12-07

4. The Impact of Leukemia on the Detection of Short Tandem Repeat (STR) Markers;Cureus;2022-11-01

5. Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran;Journal of Molecular Neuroscience;2021-01-22