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 *

118 related articles for article (PubMed ID: 38660861)

  • 1. [Cases Analysis of Hemoglobin H Disease Caused by
    Wang QH; Chen XY; Tang N; Yan TZ; Huang J; Zhong QY; Luo SQ
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2024 Apr; 32(2):520-524. PubMed ID: 38660861
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene
    Chen X; Luo S; Huang J; Yuan D; Yan T; Cai R; Tang N
    Hemoglobin; 2020 Jan; 44(1):51-54. PubMed ID: 31933393
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [A case with α-thalassemia caused by novel start codon variant in conjunct with right deletion variant of α2-globin gene].
    Chen Y; Wang J; Wang C; Chen S; Feng N; Liu H; Tang X; Zhang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Jan; 38(1):12-14. PubMed ID: 33423249
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Molecular Diagnosis and Pedigree Analysis of Rare Mutations in Non-coding Region of
    Chen LZ; Yan TZ; Huang J; Zhong QY; Qin X; Tang N; Luo SQ
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2024 Jun; 32(3):940-944. PubMed ID: 38926992
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Nondeletional α-Thalassemia: Two New Mutations on the α2 Gene.
    Ropero P; Arbeteta J; Nieto JM; González FA; González B; Villegas A; Benavente C
    Hemoglobin; 2020 Jan; 44(1):17-19. PubMed ID: 32000548
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and - -
    Zhang Q; Fan X; Xu M; Zhang Y; Xu H; Wen X; Zhou W
    Hemoglobin; 2017 May; 41(3):189-192. PubMed ID: 28950779
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pedigree Analysis of Nonhomologous Sequence Recombination of
    Luo SQ; Chen XY; Tang N; Huang J; Zhong QY; Cai R; Yan TZ
    Hemoglobin; 2020 Sep; 44(5):329-333. PubMed ID: 32811243
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Heterozygosity for the Novel
    Forouzesh Pour F; Karimi K; Ghaderi Z; Tavakoli Koudehi A; Najmabadi H
    Hemoglobin; 2020 Nov; 44(6):423-426. PubMed ID: 33054440
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
    Viprakasit V; Ekwattanakit S; Chalaow N; Riolueang S; Wijit S; Tanyut P; Chat-Uthai N; Tachavanich K
    Acta Haematol; 2014; 131(2):88-94. PubMed ID: 24081251
    [TBL] [Abstract][Full Text] [Related]  

  • 10. α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region.
    Al-Riyami AZ; Daar S; Kindi SA; Madhani AA; Wali Y; Rawahi MA; Zadjali SA
    Hemoglobin; 2020 Jan; 44(1):20-26. PubMed ID: 32019385
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [The value of combined detection of HbA2 and HbF for the screening of thalassemia among individuals of childbearing ages].
    Zhuang Q; Wang G; Wang Y; Zhuang J; Jiang Y; Huang H; Xu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jan; 39(1):16-20. PubMed ID: 34964959
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia.
    Alauddin H; Kamarudin K; Loong TY; Azma RZ; Ithnin A; Jalil N; Razak NF; Koh-Xuan-Rong D; Ismail E; C-Khai L; Abdul Latiff Z; Alias H; Othman A
    Hemoglobin; 2018 Jul; 42(4):247-251. PubMed ID: 30623696
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Uncommon Combination of Hemoglobin Jax and Hemoglobin Constant Spring Leading to Microcytic Anemia.
    Srichairatanakool S; Chai-Adisaksopha C; Tantiworawit A; Phusua A; Charoenkwan P
    Am J Case Rep; 2024 May; 25():e943560. PubMed ID: 38725231
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Henderson SJ; Timbs AT; McCarthy J; Gallienne AE; Proven M; Rugless MJ; Lopez H; Eglinton J; Dziedzic D; Beardsall M; Khalil MS; Old JM
    Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of the Types of Thalassemia Gene Mutations in Nanping Area of Fujian, China].
    Chen MF; Huang MZ; Lin Q; Huang J; Chen F; Zhang JY; Xue F
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2020 Jun; 28(3):918-926. PubMed ID: 32552958
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A).
    Waye JS; Eng B; Hanna M; Hohenadel BA; Nakamura L; Walker L
    Hemoglobin; 2016 Sep; 40(5):369-370. PubMed ID: 27821014
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern Iran.
    Derakhshan SM; Khaniani MS; Afkhami F; PourFeizi AH
    Hemoglobin; 2016 Sep; 40(5):319-322. PubMed ID: 27690152
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Novel Frameshift Mutation(
    Pan L; Wang Y; Lin H; Zhang X; Zhang R
    Hemoglobin; 2024 May; 48(3):200-202. PubMed ID: 38653553
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Haemoglobinopathies that occur with decreased HbA2 levels: a gene mutation set involving the δ gene at a Spanish centre.
    Villegas A; González FA; Nieto JM; de la Fuente-Gonzalo F; Martínez R; Torrejón MJ; Ropero P
    J Clin Pathol; 2017 Jan; 70(1):75-80. PubMed ID: 27387985
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.