BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

311 related articles for article (PubMed ID: 22896714)

  • 21. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS; He J; Zhang J; Zeng XH; Su J; Xu XH; Li SY; Chen H; Zhang YH
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage.
    Parks M; Court S; Bowns B; Cleary S; Clokie S; Hewitt J; Williams D; Cole T; MacDonald F; Griffiths M; Allen S
    Eur J Hum Genet; 2017 Apr; 25(4):416-422. PubMed ID: 28120840
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Haplotype-Assisted Noninvasive Prenatal Diagnosis of Genetic Diseases by Massively Parallel Sequencing of Maternal Plasma Cell-Free DNA.
    Ju J; Su F; Chen C; Sun J; Gao Y
    Methods Mol Biol; 2023; 2590():287-294. PubMed ID: 36335505
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing.
    Ma D; Ge H; Li X; Jiang T; Chen F; Zhang Y; Hu P; Chen S; Zhang J; Ji X; Xu X; Jiang H; Chen M; Wang W; Xu Z
    Gene; 2014 Jul; 544(2):252-8. PubMed ID: 24768736
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Non-invasive prenatal diagnosis using fetal DNA in maternal plasma: a preliminary study for identification of paternally-inherited alleles using single nucleotide polymorphisms.
    Chen JJ; Tan JA; Chua KH; Tan PC; George E
    BMJ Open; 2015 Jul; 5(7):e007648. PubMed ID: 26201722
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Non-invasive prenatal testing of beta-hemoglobinopathies using next generation sequencing, in-silico sequence size selection, and haplotyping.
    Erlich HA; Ko L; Lee J; Eaton K; Calloway CD; Lal A; Das R; Jamwal M; Lopez-Pena C; Mack SJ
    Croat Med J; 2024 Jun; 65(3):180-188. PubMed ID: 38868964
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Prenatal diagnosis of β-thalassaemia using cell-free fetal DNA in maternal plasma].
    Li GH; Rong KB; Luo YF; Chen D; Gong CP; Wu J; DI YW; Ge YF
    Nan Fang Yi Ke Da Xue Xue Bao; 2011 Aug; 31(8):1437-9. PubMed ID: 21868341
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Non-invasive prenatal diagnosis of beta-thalassemia by semiconductor sequencing: a feasibility study in the sardinian population.
    Saba L; Masala M; Capponi V; Marceddu G; Massidda M; Rosatelli MC
    Eur J Hum Genet; 2017 May; 25(5):600-607. PubMed ID: 28272531
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Development of a PCR/LDR/capillary electrophoresis assay with potential for the detection of a beta-thalassemia fetal mutation in maternal plasma.
    Yi P; Chen Z; Yu L; Zheng Y; Liu G; Xie H; Zhou Y; Zheng X; Han J; Li L
    J Matern Fetal Neonatal Med; 2010 Aug; 23(8):920-7. PubMed ID: 20121392
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Haplotypes inside the beta-globin gene: use as new biomarkers for beta-thalassemia prenatal diagnosis in north of Iran.
    Hashemi-Soteh MB; Mousavi SS; Tafazoli A
    J Biomed Sci; 2017 Dec; 24(1):92. PubMed ID: 29202846
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations.
    Zeevi DA; Altarescu G; Weinberg-Shukron A; Zahdeh F; Dinur T; Chicco G; Herskovitz Y; Renbaum P; Elstein D; Levy-Lahad E; Rolfs A; Zimran A
    J Clin Invest; 2015 Oct; 125(10):3757-65. PubMed ID: 26426075
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma.
    Lun FM; Tsui NB; Chan KC; Leung TY; Lau TK; Charoenkwan P; Chow KC; Lo WY; Wanapirak C; Sanguansermsri T; Cantor CR; Chiu RW; Lo YM
    Proc Natl Acad Sci U S A; 2008 Dec; 105(50):19920-5. PubMed ID: 19060211
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Noninvasive prenatal diagnosis for pregnancies at risk for β-thalassaemia: a retrospective study.
    Lv W; Linpeng S; Li Z; Liang D; Jia Z; Meng D; Cram DS; Zhu H; Teng Y; Yin A; Wu L
    BJOG; 2021 Jan; 128(2):448-457. PubMed ID: 32363759
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Detection of paternally inherited fetal point mutations for β-thalassemia in maternal plasma using simple fetal DNA enrichment protocol with or without whole genome amplification: an accuracy assessment.
    Ramezanzadeh M; Salehi M; Farajzadegan Z; Kamali S; Salehi R
    J Matern Fetal Neonatal Med; 2016; 29(16):2645-9. PubMed ID: 26553322
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma.
    New MI; Tong YK; Yuen T; Jiang P; Pina C; Chan KC; Khattab A; Liao GJ; Yau M; Kim SM; Chiu RW; Sun L; Zaidi M; Lo YM
    J Clin Endocrinol Metab; 2014 Jun; 99(6):E1022-30. PubMed ID: 24606108
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Noninvasive Prenatal Diagnosis of Beta-Thalassemia Disease by Using Digital PCR Analysis of Cell-Free Fetal DNA in Maternal Plasma.
    Charoenkwan P; Traisrisilp K; Sirichotiyakul S; Phusua A; Sanguansermsri T; Tongsong T
    Fetal Diagn Ther; 2022; 49(11-12):468-478. PubMed ID: 36574763
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Noninvasive prenatal diagnosis experience in the Çukurova Region of Southern Turkey: detecting paternal mutations of sickle cell anemia and β-thalassemia in cell-free fetal DNA using high-resolution melting analysis.
    Yenilmez ED; Tuli A; Evrüke IC
    Prenat Diagn; 2013 Nov; 33(11):1054-62. PubMed ID: 23836351
    [TBL] [Abstract][Full Text] [Related]  

  • 40. MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis.
    Ding C; Chiu RW; Lau TK; Leung TN; Chan LC; Chan AY; Charoenkwan P; Ng IS; Law HY; Ma ES; Xu X; Wanapirak C; Sanguansermsri T; Liao C; Ai MA; Chui DH; Cantor CR; Lo YM
    Proc Natl Acad Sci U S A; 2004 Jul; 101(29):10762-7. PubMed ID: 15247415
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.