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 *

335 related articles for article (PubMed ID: 14296925)

  • 21. [HEMOGLOBINOPATHY SC; CLINICO-HEMATOLOGICAL STUDY OF 8 CASES].
    DE ARAUJO JT; DA PITOMBEIRA MS; JAMRA M; MANISSADJIAN A; DE PENNA HA
    Rev Hosp Clin Fac Med Sao Paulo; 1965; 20():157-64. PubMed ID: 14348717
    [No Abstract]   [Full Text] [Related]  

  • 22. [ABNORMAL HEMOGLOBINS AND HEMOGLOBINOPATHIES].
    NEIMANN N; MANCIAUX M; VERT P
    Med Infant (Paris); 1965 Feb; 72():85-92. PubMed ID: 14300343
    [No Abstract]   [Full Text] [Related]  

  • 23. Abnormal human haemoglobins. VI. The chemical difference between haemoglobins A and E.
    HUNT JA; INGRAM VM
    Biochim Biophys Acta; 1961 May; 49():520-36. PubMed ID: 13716853
    [No Abstract]   [Full Text] [Related]  

  • 24. [DESCRIPTION OF A NEW SLOW HEMOGLOBIN IN A CASERTIAN FAMILY (HB CASERTA)].
    VENTRUTO V; DEROSA L; BIANCHI P; RICCHI L; QUATTRIN N
    Prog Med (Napoli); 1964 Mar; 20():157-62. PubMed ID: 14216869
    [No Abstract]   [Full Text] [Related]  

  • 25. THE CHARACTERIZATION OF HEMOGLOBIN SHIMONOSEKI.
    HANADA M; RUCKNAGEL DL
    Blood; 1964 Nov; 24():624-35. PubMed ID: 14236737
    [No Abstract]   [Full Text] [Related]  

  • 26. Abnormal human haemoglobins. V. Chemical investigation of haemoglobins A, G, C, X from one individual.
    BAGLIONI C; INGRAM VM
    Biochim Biophys Acta; 1961 Apr; 48():253-65. PubMed ID: 13685865
    [No Abstract]   [Full Text] [Related]  

  • 27. CURRENT CONCEPTS OF THE GENETICS OF THALASSEMIA.
    RUCKNAGEL DL
    Ann N Y Acad Sci; 1964 Oct; 119():436-49. PubMed ID: 14219424
    [No Abstract]   [Full Text] [Related]  

  • 28. HEMOLYTIC DISEASE ASSOCIATED WITH THE PRODUCTION OF ABNORMAL HEMOGLOBIN AND INTRAERYTHROCYTIC HEINZ BODIES.
    SHIBATA S; IUCHI I; MIYAJI T; UEDA S; TAKEDA I
    Nihon Ketsueki Gakkai Zasshi; 1963 Apr; 26():164-73. PubMed ID: 14043483
    [No Abstract]   [Full Text] [Related]  

  • 29. MOLAR EXTINCTION COEFFICIENTS OF HEMOGLOBIN M-IWATE, WITH A NE M-IWATE, WITH A NOTE ON THE SPECTROPHOTOMETRIC DETERMINATION OF THIS HEMOGLOBIN IN THE HEMOLYSATE OF HEREDITARY NIGREMIA.
    SHIBATA S; IUCHI I; MIYAJI T; TAMURA A
    Nihon Ketsueki Gakkai Zasshi; 1963 Nov; 26():641-9. PubMed ID: 14119158
    [No Abstract]   [Full Text] [Related]  

  • 30. [ABNORMAL HEMOGLOBINS AND THEIR FREQUENCY IN THE PO DELTA].
    ORTOLANI M
    Minerva Med; 1964 May; 55():SUPPL:1564-9. PubMed ID: 14164593
    [No Abstract]   [Full Text] [Related]  

  • 31. HEMOGLOBIN SHIMOSEKI (ALPHA-2-53ARG BETA-2-A), A SLOW-MOVING HEMOGLOBIN FOUND IN A JAPANESE FAMILY, WITH SPECIAL REFERENCE TO ITS CHEMISTRY.
    MIYAJI T; IUCHI I; TAKEDA I; SHIBATA S
    Nihon Ketsueki Gakkai Zasshi; 1963 Oct; 26():531-7. PubMed ID: 14095682
    [No Abstract]   [Full Text] [Related]  

  • 32. [COMPARATIVE OBSERVATION OF NORMAL AND ABNORMAL HUMAN HEMOGLOBINS].
    RUCKPAUL K; STOPP G
    Dtsch Gesundheitsw; 1964 Aug; 19():1580-5. PubMed ID: 14308928
    [No Abstract]   [Full Text] [Related]  

  • 33. HEMOGLOBIN-H DISEASE WITH PERSISTENT HEMOGLOBIN "BART'S" IN A JEWISH FAMILY OF ALEPPO-URFALIAN ANCESTRY.
    ZLOTNICK A; RAMOT B; HAMOSH P
    Isr Med J; 1964; 23():57-63. PubMed ID: 14173527
    [No Abstract]   [Full Text] [Related]  

  • 34. THREE INHERITED INTRA-ERYTHROCYTIC DEFECTS: HEREDITARY SPHEROCYTOSIS, HB S AND HB C.
    THOMPSON RB; ROBERTSON MG
    Acta Haematol; 1964 Oct; 32():233-8. PubMed ID: 14252557
    [No Abstract]   [Full Text] [Related]  

  • 35. HEMOGLOBIN MARHUS. I. CLINICAL FAMILY STUDY.
    HOBOLTH N
    Acta Paediatr Scand; 1965 Jul; 54():355-62. PubMed ID: 14343445
    [No Abstract]   [Full Text] [Related]  

  • 36. [ON A CASE OF DOUBLE DREPANOCYTOSIS-MICROCYTHEMIA HETEROZYGOSITY WITH DIMINUTION OF FRACTION A2].
    CUTILLO S; MIRAGLIADELGIUDICE M; DEBELLIS U
    Rass Int Clin Ter; 1963 Dec; 43():1251-64. PubMed ID: 14129142
    [No Abstract]   [Full Text] [Related]  

  • 37. Study of blood groups, abnormal hemoglobins and other genetical characters in some tribes of Gujarat.
    Vyas GN; Bhatia HM; Sukumaran PK; Balkrishnan V; Sanghvi LD
    Am J Phys Anthropol; 1962 Sep; 20(3):255-65. PubMed ID: 13998076
    [No Abstract]   [Full Text] [Related]  

  • 38. [THE EVOLUTION OF THE GENETIC PROBLEM IN THALASSEMIA].
    GATTO I
    Pediatria (Napoli); 1964 Jun; 72():361-422. PubMed ID: 14170504
    [No Abstract]   [Full Text] [Related]  

  • 39. SEPARATION OF ABNORMAL HAEMOGLOBINS.
    GEORGE WH
    Lancet; 1965 Aug; 2(7409):446-7. PubMed ID: 14348612
    [No Abstract]   [Full Text] [Related]  

  • 40. DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
    HUEHNS ER; HECHT F; KEIL JV; MOTULSKY AG
    Proc Natl Acad Sci U S A; 1964 Jan; 51(1):89-97. PubMed ID: 14104609
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.