These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 25863092)

  • 1. [Diagnosis and prenatal diagnosis to a family of hemoglobin variant with α-thalassemia].
    Du L; Wu J; Qin D; Wang J; Luo M; Guo H; Yuan T; Zhang Y; Wang Y; Yin A
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):226-8. PubMed ID: 25863092
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
    Srivorakun H; Fucharoen G; Sae-Ung N; Sanchaisuriya K; Ratanasiri T; Fucharoen S
    Eur J Haematol; 2009 Jul; 83(1):57-65. PubMed ID: 19226360
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Prenatal diagnosis of Thailand deletion of alpha-thalassemia 1].
    Chen P; Li SQ; Li MQ; Pang LH; Lin WX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):247-50. PubMed ID: 17557230
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Homozygous alpha-thalassemia-1 presenting in a fetus without anemia.
    Yang Y; Li DZ
    Acta Haematol; 2010; 123(4):207-9. PubMed ID: 20395676
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (- -
    Yang X; Yan JM; Li J; Xie XM; Zhou JY; Li Y; Li DZ
    Hemoglobin; 2016 Sep; 40(5):353-355. PubMed ID: 27686733
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
    Karnpean R; Fucharoen G; Fucharoen S; Sae-ung N; Sanchaisuriya K; Ratanasiri T
    Acta Haematol; 2009; 121(4):227-33. PubMed ID: 19546525
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.
    Li D; Liao C; Li J; Xie X; Huang Y; Zhong H
    Haematologica; 2006 May; 91(5):649-51. PubMed ID: 16627247
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comparison of red blood cell hematology among normal, alpha-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy.
    Srisupundit K; Piyamongkol W; Tongsong T
    Am J Hematol; 2008 Dec; 83(12):908-10. PubMed ID: 18932192
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of nondeletional α-thalassemia in a prenatal screening program by reverse dot-blot in southern China.
    Li J; Li R; Li DZ
    Hemoglobin; 2015; 39(1):42-5. PubMed ID: 25523870
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].
    Li Q; Li LY; Mo QH
    Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jan; 28(1):16-9. PubMed ID: 18227017
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of rare thalassemia caused by HS-40 regulatory site deletion.
    Luo S; Chen X; Zhong Q; Wang Q; Xu Z; Qin L; Wang J; Yuan D; Yan T; Tang N
    Hematology; 2020 Dec; 25(1):286-291. PubMed ID: 32720864
    [No Abstract]   [Full Text] [Related]  

  • 13. Treatment of alpha(0)-thalassemia (--(SEA)/--(SEA)) via serial fetal and post-natal transfusions: Can early fetal intervention improve outcomes?
    Chmait RH; Baskin JL; Carson S; Randolph LM; Hamilton A
    Hematology; 2015 May; 20(4):217-22. PubMed ID: 25116001
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Molecular screening and prenatal diagnosis of the deletional alpha-thalassemia by polymerase chain reaction amplification].
    Xu XM; Cai XH; Li J
    Zhonghua Yi Xue Za Zhi; 1994 Aug; 74(8):495-7, 520. PubMed ID: 7994662
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Prenatal gene diagnosis of paternally inherited alpha-thalassemia by detecting fetal DNA in maternal plasma].
    Chen P; Li MJ; Li MQ; Li SQ; Zhou LY; Lin WX
    Zhonghua Yi Xue Za Zhi; 2007 Jun; 87(22):1540-4. PubMed ID: 17785106
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N; Pinmuang-Ngam C; Fucharoen G; Fucharoen S
    Fetal Diagn Ther; 2007; 22(4):264-8. PubMed ID: 17369692
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of a rare β-thalassemia gene －90 (C>T) (HBB: c.-140 C>T) mutation associated with deletional Hb H disease (--
    Qian H; Huang J; Xu J; Zhao W; Ye X; Liu W
    Mol Genet Genomic Med; 2020 Nov; 8(11):e1472. PubMed ID: 32885601
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cord blood analysis for rapid prenatal confirmation of Hb Bart's disease using the Sebia Capillary electrophoresis system.
    Liao C; Zhou JY; Xie XM; Li R; Li DZ
    Hemoglobin; 2012; 36(2):186-91. PubMed ID: 22191698
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Carrier screening and prenatal diagnosis for alpha-thalassemia with biphasic polymerase chain reaction.
    Kuo PL; Lin TM; Huang KF; Yeh NG; Wu DB; Wu RC; Tzeng CC; Wu HL; Huang KE
    J Formos Med Assoc; 1994 Sep; 93(9):765-9. PubMed ID: 7735005
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rapid prenatal diagnosis of Hb Bart's hydrops fetalis in southeast Asia area by polymerase chain reaction.
    Chang JG; Chen CP; Ho HJ; Lin CP; Lee LS; Chen PH
    Int J Hematol; 1992 Oct; 56(2):155-9. PubMed ID: 1421177
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.