224 related articles for article (PubMed ID: 26201722)
41. Noninvasive prenatal diagnosis of beta-thalassaemia using individual fetal erythroblasts isolated from maternal blood after enrichment.
Kolialexi A; Vrettou C; Traeger-Synodinos J; Burgemeister R; Papantoniou N; Kanavakis E; Antsaklis A; Mavrou A
Prenat Diagn; 2007 Dec; 27(13):1228-32. PubMed ID: 17987605
[TBL] [Abstract][Full Text] [Related]
42. High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh.
Islam MT; Sarkar SK; Sultana N; Begum MN; Bhuyan GS; Talukder S; Muraduzzaman AKM; Alauddin M; Islam MS; Biswas PP; Biswas A; Qadri SK; Shirin T; Banu B; Sadya S; Hussain M; Sarwardi G; Khan WA; Mannan MA; Shekhar HU; Chowdhury EK; Sajib AA; Akhteruzzaman S; Qadri SS; Qadri F; Mannoor K
BMC Genet; 2018 Jan; 19(1):1. PubMed ID: 29295702
[TBL] [Abstract][Full Text] [Related]
43. The molecular characterization of Beta globin gene in thalassemia patients reveals rare and a novel mutations in Pakistani population.
Yasmeen H; Toma S; Killeen N; Hasnain S; Foroni L
Eur J Med Genet; 2016 Aug; 59(8):355-62. PubMed ID: 27263053
[TBL] [Abstract][Full Text] [Related]
44. Fetal Genotyping in Maternal Blood by Digital PCR: Towards NIPD of Monogenic Disorders Independently of Parental Origin.
Perlado S; Bustamante-Aragonés A; Donas M; Lorda-Sánchez I; Plaza J; Rodríguez de Alba M
PLoS One; 2016; 11(4):e0153258. PubMed ID: 27078875
[TBL] [Abstract][Full Text] [Related]
45. Identification of three new nucleotide substitutions in the β-globin gene: laboratoristic approach and impact on genetic counselling for beta-thalassaemia.
Vinciguerra M; Passarello C; Leto F; Cassarà F; Cannata M; Maggio A; Giambona A
Eur J Haematol; 2014; 92(5):444-9. PubMed ID: 24401016
[TBL] [Abstract][Full Text] [Related]
46. [Genotype of thalassemia genes and the polymorphism of β- globin gene in Cantonese].
Liu L; Jiang WY; Xu SY; Chen J; Chen LM; Tian QH; Wang JC
Zhonghua Xue Ye Xue Za Zhi; 2013 Jul; 34(7):595-9. PubMed ID: 23906453
[TBL] [Abstract][Full Text] [Related]
47. Reliable detection of paternal SNPs within deletion breakpoints for non-invasive prenatal exclusion of homozygous α-thalassemia in maternal plasma.
Yan TZ; Mo QH; Cai R; Chen X; Zhang CM; Liu YH; Chen YJ; Zhou WJ; Xiong F; Xu XM
PLoS One; 2011; 6(9):e24779. PubMed ID: 21980356
[TBL] [Abstract][Full Text] [Related]
48. Clinical application of a protocol based on universal next-generation sequencing for the diagnosis of beta-thalassaemia and sickle cell anaemia in preimplantation embryos.
Kubikova N; Babariya D; Sarasa J; Spath K; Alfarawati S; Wells D
Reprod Biomed Online; 2018 Aug; 37(2):136-144. PubMed ID: 29853423
[TBL] [Abstract][Full Text] [Related]
49. Molecular genetics and prenatal diagnosis of beta thalassemia to control transfusion dependent births in carrier Pakistani couples.
Kanwal S; Bukhari S; Perveen S
J Pak Med Assoc; 2017 Jul; 67(7):1030-1034. PubMed ID: 28770881
[TBL] [Abstract][Full Text] [Related]
50. Noninvasive prenatal diagnostic assay for the detection of beta-thalassemia.
Papasavva T; Kalakoutis G; Kalikas I; Neokli E; Papacharalambous S; Kyrri A; Kleanthous M
Ann N Y Acad Sci; 2006 Sep; 1075():148-53. PubMed ID: 17108205
[TBL] [Abstract][Full Text] [Related]
51. Prenatal Diagnosis of β-thalassemia with Cell-free Fetal DNA in Maternal Plasma.
Zhao L; Liang X; Huang H; Lan H; Wu X; Wang C
J Coll Physicians Surg Pak; 2019 May; 29(5):483-485. PubMed ID: 31036126
[TBL] [Abstract][Full Text] [Related]
52. Non-invasive prenatal diagnosis of β-thalassemia by detection of the cell-free fetal DNA in maternal circulation: a systematic review and meta-analysis.
Zafari M; Kosaryan M; Gill P; Alipour A; Shiran M; Jalalli H; Banihashemi A; Fatahi F
Ann Hematol; 2016 Aug; 95(8):1341-50. PubMed ID: 26968552
[TBL] [Abstract][Full Text] [Related]
53. Prenatal diagnosis of beta-thalassaemia by coelocentesis.
Makrydimas G; Georgiou I; Kranas V; Zikopoulos K; Lolis D
Mol Hum Reprod; 1997 Aug; 3(8):729-31. PubMed ID: 9294859
[TBL] [Abstract][Full Text] [Related]
54. Noninvasive prenatal diagnosis of β-thalassemia by relative haplotype dosage without analyzing proband.
Li H; Du B; Jiang F; Guo Y; Wang Y; Zhang C; Zeng X; Xie Y; Ouyang S; Xian Y; Chen M; Liu W; Sun X
Mol Genet Genomic Med; 2019 Nov; 7(11):e963. PubMed ID: 31566929
[TBL] [Abstract][Full Text] [Related]
55. Combined use of gap-PCR and next-generation sequencing improves thalassaemia carrier screening among premarital adults in China.
Zhao J; Li J; Lai Q; Yu Y
J Clin Pathol; 2020 Aug; 73(8):488-492. PubMed ID: 31980563
[TBL] [Abstract][Full Text] [Related]
56. Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma.
Li Y; Di Naro E; Vitucci A; Zimmermann B; Holzgreve W; Hahn S
JAMA; 2005 Feb; 293(7):843-9. PubMed ID: 15713774
[TBL] [Abstract][Full Text] [Related]
57. Prenatal diagnosis of beta-thalassaemia: experience in a developing country.
Saxena R; Jain PK; Thomas E; Verma IC
Prenat Diagn; 1998 Jan; 18(1):1-7. PubMed ID: 9483634
[TBL] [Abstract][Full Text] [Related]
58. Co-inheritance of alpha-and beta-thalassemia in Khuzestan Province, Iran.
Rahim F; Kaikhaei B; Zandian K; Hoseini A
Hematology; 2008 Feb; 13(1):59-64. PubMed ID: 18534068
[TBL] [Abstract][Full Text] [Related]
59. The use of Taqman genotyping assays for rapid confirmation of β-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations.
Teh LK; Lee TY; Tan JA; Lai MI; George E
Int J Lab Hematol; 2015 Feb; 37(1):79-89. PubMed ID: 24725998
[TBL] [Abstract][Full Text] [Related]
60. Challenges in prenatal diagnosis of beta thalassaemia: couples with normal HbA2 in one partner.
Gorivale M; Sawant P; Mehta P; Nadkarni A; Ghosh K; Colah R
Prenat Diagn; 2015 Dec; 35(13):1353-7. PubMed ID: 26456238
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
