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 *

121 related articles for article (PubMed ID: 472974)

  • 1. [H-haemoglobin disease in Costa Rica (author's transl)].
    Saenz GF; Jiménez E; Mora L
    Sangre (Barc); 1979; 24(3):333-9. PubMed ID: 472974
    [No Abstract]   [Full Text] [Related]  

  • 2. [Haemoglobin H disease. Third form of alfa-thalassaemia found in Colombia (author's transl)].
    Echavarria A; Molina C; Angel M
    Sangre (Barc); 1976; 21(1):43-53. PubMed ID: 1265589
    [No Abstract]   [Full Text] [Related]  

  • 3. [Haemoglobin H disease. Report of two Peruvian families (author's transl)].
    Jeri A; Rojas M; Castillo J
    Sangre (Barc); 1976; 21(1):67-76. PubMed ID: 1265592
    [No Abstract]   [Full Text] [Related]  

  • 4. [Drepanocytic syndromes in Costa Rica. IV. Double heterozigous S/alpha thalassaemia syndrome (author's transl)].
    Saenz GF; Elizondo J; Arroyo G; Jiménez J; Montero G
    Sangre (Barc); 1979; 24(2):205-10. PubMed ID: 462337
    [No Abstract]   [Full Text] [Related]  

  • 5. [Investigation on a family with alpha-thalassemia (author's transl)].
    Pereira JM; Callado AN; Monteiro AL; Bastos RM; da Pinto A; Lirio AS
    Rev Bras Pesqui Med Biol; 1973; 6(6):349-53. PubMed ID: 4791745
    [No Abstract]   [Full Text] [Related]  

  • 6. [Observations of alpha-thalasemia and hemoglobin h in spaniards (author's transl)].
    Villegas A; Pérez Gutiérrez A; Díaz Mediavilla J; Espinos D
    Sangre (Barc); 1979; 24(6):1088-102. PubMed ID: 538560
    [No Abstract]   [Full Text] [Related]  

  • 7. [Case of hemoglobinopathy H in an Uzbek family].
    Tokarev IuN; Chukanin NN; Settarova DA; Settarov IA; Ermakov NV
    Probl Gematol Pereliv Krovi; 1981 Sep; 26(9):53-5. PubMed ID: 6458809
    [No Abstract]   [Full Text] [Related]  

  • 8. [Haemoglobin Korle-Bu (alfa2-beta2 73 asp-asm) finding in Costa Rica (author's transl)].
    Elizondo J; Saenz GF; Alvarado Mde L; Ramon M
    Sangre (Barc); 1976; 21(1):54-6. PubMed ID: 1265590
    [No Abstract]   [Full Text] [Related]  

  • 9. The alpha thalassaemic syndrome of Hb H disease in a Sri Lankan family.
    de Tissera A; Balakumar L; Seneviratne A; Wickremasinghe P
    Ceylon Med J; 1988 Dec; 33(4):135-9. PubMed ID: 3248322
    [No Abstract]   [Full Text] [Related]  

  • 10. [Current status of the study of hemoglobinopathies in Costa Rica].
    Sáenz GF
    Sangre (Barc); 1985; 30(2):168-80. PubMed ID: 4012518
    [No Abstract]   [Full Text] [Related]  

  • 11. [Cooley's disease (beta+-thalassemia major) in Costa Rica (author's transl)].
    Saenz GF; Monge B; Arroyo G; Alvarado Mde L
    Sangre (Barc); 1976; 21(1):117-22. PubMed ID: 1265581
    [No Abstract]   [Full Text] [Related]  

  • 12. Cord blood survey for haemoglobin Barts.
    Booth K
    P N G Med J; 1981 Dec; 24(4):264-6. PubMed ID: 6951352
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A study on the biochemical genetics of abnormal hemoglobins.
    I-Tao T
    Sci Sin; 1975; 18(4):527-44. PubMed ID: 1202635
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hemolytic anaemia due to unstable hemoglobin arising from spontaneous mutation--a case report.
    Dash S; Menon S; Marwaha RK
    Indian J Pathol Microbiol; 2006 Apr; 49(2):269-70. PubMed ID: 16933736
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Finding of haemoglobin E beta 26 (B 8) glu leads to lis in Costa Rica (author's transl)].
    Saenz GF; Elizondo J; Colombo B; Alvarado M; Arroyo G; Atmetlla F
    Sangre (Barc); 1977; 22(5):652-6. PubMed ID: 905942
    [No Abstract]   [Full Text] [Related]  

  • 16. [1st cases of alpha-thalassemia in Algeria: 12 cases of hemoglobinosis H].
    Trabuchet G; Belhani M; Richard F; Hamladji RM; Benabadji M; Colonna P
    Sem Hop; 1977 Apr; 53(16):885-9. PubMed ID: 197607
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Concurrence on two siblings of three haemoglobin abnormal genes: haemoglobin S, beta-thalassaemia and hereditary persistence of foetal haemoglobin (author's transl)].
    Guerrero García R; Rosillo de León J; Landero de Ruíz N; Padilla C; Ruíz Reyes G
    Sangre (Barc); 1978; 23(5):578-86. PubMed ID: 741340
    [No Abstract]   [Full Text] [Related]  

  • 18. Letter: Alpha-thalassaemia in an Australian family.
    Wilkinson T; Kronenberg H; Hobin H
    Med J Aust; 1974 Jan; 1(1):22. PubMed ID: 4814425
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. [Hereditary anemia: genetic basis, clinical characteristics, diagnosis and treatment. WHO Workgroup].
    Bull World Health Organ; 1983; 61(2):179-98. PubMed ID: 6345012
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.