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 *

163 related articles for article (PubMed ID: 8320702)

  • 1. Frequency and clinical significance of erythrocyte genetic abnormalities in Omanis.
    White JM; Christie BS; Nam D; Daar S; Higgs DR
    J Med Genet; 1993 May; 30(5):396-400. PubMed ID: 8320702
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prevalence of classic erythrocyte polymorphisms among 749 children in southern highland Rwanda.
    Gahutu JB; Musemakweri A; Harms G; Mockenhaupt FP
    Trans R Soc Trop Med Hyg; 2012 Jan; 106(1):63-5. PubMed ID: 22018599
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and alpha and beta thalassaemia.
    White JM; Byrne M; Richards R; Buchanan T; Katsoulis E; Weerasingh K
    J Med Genet; 1986 Jun; 23(3):245-51. PubMed ID: 3723553
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary anaemias in Portugal: epidemiology, public health significance, and control.
    Martins MC; Olim G; Melo J; Magalhães HA; Rodrigues MO
    J Med Genet; 1993 Mar; 30(3):235-9. PubMed ID: 8474108
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Frequency of haemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in Basra.
    Hassan MK; Taha JY; Al-Naama LM; Widad NM; Jasim SN
    East Mediterr Health J; 2003; 9(1-2):45-54. PubMed ID: 15562732
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
    Adeyemo T; Ojewunmi O; Oyetunji A
    Pan Afr Med J; 2014; 18():71. PubMed ID: 25400838
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic Blood Disorders Survey in the Sultanate of Oman.
    Al-Riyami A; Ebrahim GJ
    J Trop Pediatr; 2003 Jul; 49 Suppl 1():i1-20. PubMed ID: 12934793
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Extended molecular spectrum of beta- and alpha-thalassemia in Oman.
    Hassan SM; Hamza N; Jaffer Al-Lawatiya F; Jaffer Mohammed A; Harteveld CL; Rajab A; Giordano PC
    Hemoglobin; 2010 Jan; 34(2):127-34. PubMed ID: 20353347
    [TBL] [Abstract][Full Text] [Related]  

  • 9. α-Thalassemia does not seem to influence erythrocyte deformability in sickle cell trait carriers.
    Vayá A; Collado S; Alis R; Vera B; Romagnoli M; Barragán E
    Hemoglobin; 2014; 38(3):165-8. PubMed ID: 24601859
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The burden and consequences of inherited blood disorders among young children in western Kenya.
    Suchdev PS; Ruth LJ; Earley M; Macharia A; Williams TN
    Matern Child Nutr; 2014 Jan; 10(1):135-44. PubMed ID: 22973867
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A community-based study of common hereditary blood disorders in Oman.
    Al-Riyami AA; Suleiman AJ; Afifi M; Al-Lamki ZM; Daar S
    East Mediterr Health J; 2001 Nov; 7(6):1004-11. PubMed ID: 15332742
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Haemoglobinopathy survey in an Eti-Turk village.
    Ozsoylu S; Sahinoglu M
    Hum Hered; 1975; 25(1):50-9. PubMed ID: 1150294
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Heterogeneity and variation of clinical and haematological expression of haemoglobin S in Saudi Arabs.
    el-Hazmi MA
    Acta Haematol; 1992; 88(2-3):67-71. PubMed ID: 1281601
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Subclassification of HbS syndrome: is it necessary?
    Tyagi S; Choudhry VP; Saxena R
    Clin Lab Haematol; 2003 Dec; 25(6):377-81. PubMed ID: 14641142
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sickle-cell haemoglobin and glucose-6-phosphate dehydrogenase deficiency in tribal populations of Andhra Pradesh.
    Rao PR; Goud JD
    Indian J Med Res; 1979 Nov; 70():807-13. PubMed ID: 535978
    [No Abstract]   [Full Text] [Related]  

  • 16. Appraisal of sickle-cell and thalassaemia genes in Saudi Arabia.
    el-Hazmi MA; Warsy AS
    East Mediterr Health J; 1999 Nov; 5(6):1147-53. PubMed ID: 11924103
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Thalassaemia and glucose-6-phosphate dehydrogenase screening in 13- to 14-year-old students of the Sardinian population: preliminary findings.
    Cao A; Congiu R; Sollaino MC; Desogus MF; Demartis FR; Loi D; Cau M; Galanello R
    Community Genet; 2008; 11(3):121-8. PubMed ID: 18376107
    [TBL] [Abstract][Full Text] [Related]  

  • 18. High prevalence of hemoglobin disorders and glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Republic of Guinea (West Africa).
    Millimono TS; Loua KM; Rath SL; Relvas L; Bento C; Diakite M; Jarvis M; Daries N; Ribeiro LM; Manco L; Kaeda JS
    Hemoglobin; 2012; 36(1):25-37. PubMed ID: 21929367
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prevalence of hemoglobin E, alpha-thalassemia and glucose-6-phosphate dehydrogenase deficiency in 1,000 cord bloods studied in Bangkok.
    Tanphaichitr VS; Mahasandana C; Suvatte V; Yodthong S; Pung-amritt P; Seeloem J
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():271-4. PubMed ID: 8629122
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Frequencies of sickle cell trait and glucose-6-phosphate dehydrogenase deficiency differ in highland and nearby lowland malaria-endemic areas of Kenya.
    Moormann AM; Embury PE; Opondo J; Sumba OP; Ouma JH; Kazura JW; John CC
    Trans R Soc Trop Med Hyg; 2003; 97(5):513-4. PubMed ID: 15307413
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.