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.
2. [Prenatal diagnosis: molecular basis and techniques used in the diagnosis of monogenic hereditary diseases]. Villegas Martínez A An Med Interna; 1989 May; 6(5):227-9. PubMed ID: 2577487 [No Abstract] [Full Text] [Related]
3. Prenatal diagnosis of hemoglobinopathies by DNA analysis. Boehm C; Kazazian HH Crit Rev Oncol Hematol; 1985; 4(2):155-67. PubMed ID: 2998637 [TBL] [Abstract][Full Text] [Related]
4. Some clinical implications of recombinant DNA technology with emphasis on prenatal diagnosis of hemoglobinopathies. Anderson A Clin Biochem; 1984 Apr; 17(2):112-9. PubMed ID: 6329548 [TBL] [Abstract][Full Text] [Related]
5. [Use of DNA restriction fragment length polymorphisms in the diagnosis of genetically determined diseases]. Zietkiewicz E; Latos-Bieleńska AM; Słomski R Pol Arch Med Wewn; 1985 Oct; 74(4):269-78. PubMed ID: 2907124 [No Abstract] [Full Text] [Related]
6. [Prenatal diagnosis of hereditary hemoglobinopathies]. Cao A; Pirastu M; Rosatelli C Haematologica; 1989 Oct; 74(5 Suppl):213-22. PubMed ID: 2574134 [No Abstract] [Full Text] [Related]
7. Gene probes: application to prenatal and postnatal diagnosis of genetic disease. Kazazian HH Clin Chem; 1985 Sep; 31(9):1509-13. PubMed ID: 2992840 [TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of inherited hemoglobinopathies. Cao A; Leoni GB; Sardu R; Pischedda MC; Saba L Recenti Prog Med; 1992 Apr; 83(4):224-32. PubMed ID: 1626118 [TBL] [Abstract][Full Text] [Related]
9. Polymorphism of DNA sequence in the beta-globin gene region. Application to prenatal diagnosis of beta 0 thalassemia in Sardinia. Kan YW; Lee KY; Furbetta M; Angius A; Cao A N Engl J Med; 1980 Jan; 302(4):185-8. PubMed ID: 6927915 [TBL] [Abstract][Full Text] [Related]
10. The intrauterine diagnosis of hemoglobin disorders. Wong SC; Ali MA; Benzie R Clin Perinatol; 1984 Jun; 11(2):283-308. PubMed ID: 6086205 [TBL] [Abstract][Full Text] [Related]
12. [Use of DNA polymorphism in the diagnosis of human genetic diseases]. Cebrat S Postepy Hig Med Dosw; 1988; 42(5):461-82. PubMed ID: 2908211 [No Abstract] [Full Text] [Related]
13. Prenatal diagnosis of hemoglobinopathies: development of methods for study of fetal red cells and fibroblasts. Alter BP Am J Pediatr Hematol Oncol; 1983; 5(4):378-85. PubMed ID: 6322608 [TBL] [Abstract][Full Text] [Related]
14. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A. Kogan SC; Doherty M; Gitschier J N Engl J Med; 1987 Oct; 317(16):985-90. PubMed ID: 3657865 [TBL] [Abstract][Full Text] [Related]
15. Carrier detection and prenatal diagnosis of hemoglobinopathies in Ontario. Waye JS; Eng B; Cai SP; Patterson M; Smith J; Tang W; Chui DH Clin Invest Med; 1993 Oct; 16(5):358-71. PubMed ID: 8261689 [TBL] [Abstract][Full Text] [Related]
19. Molecular biologic diagnosis of the hemoglobinopathies. Schwartz E; Surrey S Hosp Pract (Off Ed); 1986 Sep; 21(9):163-78. PubMed ID: 3091617 [No Abstract] [Full Text] [Related]
20. DNA techniques in prenatal diagnosis and in genetic pathology. Rehder H; Friedrich U Am J Med Genet Suppl; 1987; 3():1-14. PubMed ID: 2897201 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]