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Journal Abstract Search
234 related items for PubMed ID: 2907124
1. [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]
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]
4. [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]
5. Experience of a molecular genetics service in prenatal diagnosis by DNA analysis. Trent RJ, Volpato F, Wallace RC, Lindeman R, Yakas J. Pathology; 1990 Jul; 22(3):165-8. PubMed ID: 2243730 [Abstract] [Full Text] [Related]
12. [Prenatal diagnosis in clinical practice]. González-Ramos M. Bol Med Hosp Infant Mex; 1974 Jun; 31(4):653-63. PubMed ID: 4425550 [No Abstract] [Full Text] [Related]
13. The use of amniocentesis for prenatal genetic counseling. Gertner M, Hsu LY, Martin J, Hirshhorn K. Bull N Y Acad Med; 1970 Nov; 46(11):916-21. PubMed ID: 5273905 [No Abstract] [Full Text] [Related]
16. [Use of DNA polymorphism in the diagnosis of human genetic diseases]. Cebrat S. Postepy Hig Med Dosw; 1988 Nov; 42(5):461-82. PubMed ID: 2908211 [No Abstract] [Full Text] [Related]
18. Noninvasive approaches to prenatal diagnosis of hemoglobinopathies using fetal DNA in maternal plasma. Lo YM, Chiu RW. Hematol Oncol Clin North Am; 2010 Dec; 24(6):1179-86. PubMed ID: 21075287 [Abstract] [Full Text] [Related]
19. [Prenatal diagnosis of hereditary diseases (a review of the literature)]. Sviatkina OB, Kun'kina LZ. Akush Ginekol (Mosk); 1973 Apr; 49(4):11-5. PubMed ID: 4616633 [No Abstract] [Full Text] [Related]