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 *

324 related articles for article (PubMed ID: 909565)

  • 1. Identification of a nondeletion defect in alpha-thalassemia.
    Kan YW; Dozy AM; Trecartin R; Todd D
    N Engl J Med; 1977 Nov; 297(20):1081-4. PubMed ID: 909565
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.
    Bowden DK; Hill AV; Higgs DR; Oppenheimer SJ; Weatherall DJ; Clegg JB
    J Clin Invest; 1987 Jan; 79(1):39-43. PubMed ID: 3793931
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Study of the molecular causes of thalassemia. II. Deletion of alpha-globin genes in hemoglobinopathy H].
    Shipitsyna GI; Lunts MG; Shifter KA; Idel'son LI; Limborskaia SA
    Genetika; 1980; 16(1):78-85. PubMed ID: 6449401
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular characterization of severe alpha-thalassemias causing hydrops fetalis in Taiwan.
    Ko TM; Hsieh FJ; Hsu PM; Lee TY
    Am J Med Genet; 1991 Jun; 39(3):317-20. PubMed ID: 1867284
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Modification of hemoglobin H disease by sickle trait.
    Matthay KK; Mentzer WC; Dozy AM; Kan YW; Bainton DF
    J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new genetic basis for hemoglobin-H disease.
    Pressley L; Higgs DR; Clegg JB; Perrine RP; Pembrey ME; Weatherall DJ
    N Engl J Med; 1980 Dec; 303(24):1383-8. PubMed ID: 6253786
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The molecular basis of alpha-thalassemia in Thailand.
    Winichagoon P; Fucharoen S; Wasi P
    Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():7-13. PubMed ID: 1298997
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Thalassemias in Sardinia: molecular pathology, phenotype-genotype correlation, and prevention.
    Cao A; Rosatelli C; Pirastu M; Galanello R
    Am J Pediatr Hematol Oncol; 1991; 13(2):179-88. PubMed ID: 2069229
    [TBL] [Abstract][Full Text] [Related]  

  • 9. In vitro hemoglobin synthesis in the thalassemia syndromes.
    Weatherall DJ; Clegg JB
    Int Rev Exp Pathol; 1974; 13(0):117-59. PubMed ID: 4602370
    [No Abstract]   [Full Text] [Related]  

  • 10. Hemoglobin barts hydrops fetalis syndrome.
    Bowman E; Watts J; Burrows R; Chui DH
    Haematologia (Budap); 1987; 20(3):125-30. PubMed ID: 3692334
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Current views of thalassemia intermedia].
    Longinotti M; Dore F; Oggiano L; Pardini S; Pistidda P; Guiso L; Frogheri L; Bonfigli S; Murineddu M; Rimini E
    Recenti Prog Med; 1992 Apr; 83(4):233-40. PubMed ID: 1626119
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [A Japanese family with hereditary HbH disease--a case report and its gene analysis].
    Hattori Y; Yamashiro Y; Yamamoto K; Morishita M; Miyaji T; Yamamoto K; Matsuno Y; Fujii H; Miwa S; Ichimaru M
    Rinsho Ketsueki; 1990 Feb; 31(2):183-8. PubMed ID: 2329681
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.
    Embury SH; Lebo RV; Dozy AM; Kan YW
    J Clin Invest; 1979 Jun; 63(6):1307-10. PubMed ID: 447845
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.
    Lie-Injo LE; Herrera AR; Lebo RV; Hassan K; Lopez CG
    Am J Hematol; 1985 Mar; 18(3):289-96. PubMed ID: 2983536
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletion.
    Orkin SH; Alter BP; Altay C; Mahoney MJ; Lazarus H; Hobbins JC; Nathan DG
    N Engl J Med; 1978 Jul; 299(4):166-72. PubMed ID: 661890
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2.
    Galanello R; Melis MA; Maccioni L; Pirastu M; Cao A
    Pediatr Res; 1984 Feb; 18(2):158-62. PubMed ID: 6322098
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.
    Tan J; Tay JS; Wong YC; Kham SK; Bte Abd Aziz N; Teo SH; Wong HB
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():252-6. PubMed ID: 8629117
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait.
    Steinberg MH; Coleman MB; Adams JG; Hartmann RC; Saba H; Anagnou NP
    Blood; 1986 Feb; 67(2):469-73. PubMed ID: 3942832
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Silent thalassemias: genotypes and phenotypes.
    Bianco I; Cappabianca MP; Foglietta E; Lerone M; Deidda G; Morlupi L; Grisanti P; Ponzini D; Rinaldi S; Graziani B
    Haematologica; 1997; 82(3):269-80. PubMed ID: 9234571
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An alpha-globin gene initiation codon mutation in a black family with HbH disease.
    Olivieri NF; Chang LS; Poon AO; Michelson AM; Orkin SH
    Blood; 1987 Sep; 70(3):729-32. PubMed ID: 3620699
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.