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290 related items for PubMed ID: 2574134
1. [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]
3. Prenatal diagnosis of inherited hemoglobinopathies. Cao A, Pirastu M, Rosatelli C. Haematologica; 1990 Apr; 75 Suppl 5():169-77. PubMed ID: 1982278 [No Abstract] [Full Text] [Related]
4. [Prenatal diagnosis of hemoglobinopathies in the 1st and 2nd pregnancy trimesters]. Ferrari M, Cantù Rajnoldi A, Cremonesi L, Donzelli C, Pietri S, Tedeschi S, Travi M, Nicolini U, Brambati B. Pediatr Med Chir; 1984 Apr; 6(6):769-73. PubMed ID: 6545587 [Abstract] [Full Text] [Related]
5. [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]
6. Molecular biologic diagnosis of the hemoglobinopathies. Schwartz E, Surrey S. Hosp Pract (Off Ed); 1986 Sep 15; 21(9):163-78. PubMed ID: 3091617 [No Abstract] [Full Text] [Related]
7. Prenatal diagnosis of hemoglobinopathies in Ontario, Canada. Basran RK, Patterson M, Walker L, Nakamura LM, Eng B, Chui DH, Waye JS. Ann N Y Acad Sci; 2005 Sep 15; 1054():507-10. PubMed ID: 16339708 [Abstract] [Full Text] [Related]
8. Prenatal diagnosis of beta-thalassaemia and other haemoglobinopathies in India. Thakur (Mahadik) C, Vaz F, Banerjee M, Kapadia C, Natrajan PG, Yagnik H, Gangal S. Prenat Diagn; 2000 Mar 15; 20(3):194-201. PubMed ID: 10719320 [Abstract] [Full Text] [Related]
9. Diagnosis of sickle cell anemia and beta-thalassemia with enzymatically amplified DNA and nonradioactive allele-specific oligonucleotide probes. Saiki RK, Chang CA, Levenson CH, Warren TC, Boehm CD, Kazazian HH, Erlich HA. N Engl J Med; 1988 Sep 01; 319(9):537-41. PubMed ID: 3405266 [Abstract] [Full Text] [Related]
10. Noninvasive approaches to prenatal diagnosis of hemoglobinopathies using fetal DNA in maternal plasma. Lo YM, Chiu RW. Hematol Oncol Clin North Am; 2010 Dec 01; 24(6):1179-86. PubMed ID: 21075287 [Abstract] [Full Text] [Related]
11. [Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics]. Benítez J, Fernández E, Ramos C, Nunes V, del Río E, Baiget M. Rev Clin Esp; 1989 Apr 01; 184(7):364-6. PubMed ID: 2570446 [Abstract] [Full Text] [Related]
12. Prenatal diagnosis of hemoglobinopathies by using polymerase chain reaction and allele-specific oligonucleotide probes. Crisan D, Diven WF, Hartle K, Osborne PT, Mason L. Clin Chem; 1989 Sep 01; 35(9):1854. PubMed ID: 2673581 [No Abstract] [Full Text] [Related]
13. Prenatal diagnosis of hemoglobinopathies: the New England approach. Alter BP, Orkin SH, Forget BG, Nathan DG. Ann N Y Acad Sci; 1980 Sep 01; 344():151-64. PubMed ID: 6930865 [No Abstract] [Full Text] [Related]
14. Prenatal diagnosis of unusual hemoglobinopathies. Kim JH, Lebo RV, Cai SP, Su X, Chung JH, Mentzer WC, Golbus MS. Am J Med Genet; 1994 Mar 01; 50(1):15-20. PubMed ID: 8160747 [Abstract] [Full Text] [Related]
15. Molecular diagnosis of hemoglobinopathies and thalassemia. Kan YW, Chang JC. Prenat Diagn; 2010 Jul 01; 30(7):608-10. PubMed ID: 20572100 [No Abstract] [Full Text] [Related]
16. Prenatal diagnosis of inherited hemoglobinopathies. Cao A, Rosatelli C, Pirastu M. J Genet Hum; 1986 Nov 01; 34(5):413-24. PubMed ID: 3540210 [Abstract] [Full Text] [Related]
17. Chorionic villus sampling for first trimester diagnosis of beta-thalassaemia. Report of the first South African case. Ramsay M, Levin SL, Rosendorff J, Pinto M, Bernstein R. S Afr Med J; 1985 Oct 26; 68(9):672-5. PubMed ID: 4060029 [Abstract] [Full Text] [Related]
18. Prenatal diagnosis of thalassemia and of the hemoglobinopathies; a review. Loukopoulos D. Hemoglobin; 1985 Oct 26; 9(5):435-59. PubMed ID: 3910616 [Abstract] [Full Text] [Related]
19. DNA-based prenatal diagnosis of heritable skin diseases. Christiano AM, Uitto J. Arch Dermatol; 1993 Nov 26; 129(11):1455-9. PubMed ID: 7902070 [Abstract] [Full Text] [Related]
20. Direct gene analysis of chorionic villi: A possible technique for first-trimester antenatal diagnosis of haemoglobinopathies. Williamson R, Eskdale J, Coleman DV, Niazi M, Loeffler FE, Modell BM. Lancet; 1981 Nov 21; 2(8256):1125-7. PubMed ID: 6118574 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]