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11. Intrauterine diagnosis of congenital and genetic abnormalities. Cortner JA J Ark Med Soc; 1972 Nov; 69(6):178-81. PubMed ID: 4263777 [No Abstract] [Full Text] [Related]
12. Population screening for genetic disorders in California. Kaback MM UCLA Forum Med Sci; 1978; 20():207-19. PubMed ID: 80863 [No Abstract] [Full Text] [Related]
13. [Organization of the early prenatal diagnosis of chromosome aberrations and hereditary metabolic diseases]. Boué A Arch Fr Pediatr; 1974 May; 31(5):433-6. PubMed ID: 4441229 [No Abstract] [Full Text] [Related]
15. Prevention of hereditary disease. Jenkins T S Afr Med J; 1974 Jul; 48(35):1500-6. PubMed ID: 4277615 [No Abstract] [Full Text] [Related]
16. [Prenatal diagnosis of genetic diseases. Apropos of 1061 early amniocenteses]. Larget-Piet L; Larget-Piet A J Genet Hum; 1980 Sep; 28(3):233-8. PubMed ID: 7463022 [No Abstract] [Full Text] [Related]
17. The centralized prenatal genetics screening program of New York City III: The first 7,000 cases. Benn PA; Hsu LY; Carlson A; Tannenbaum HL Am J Med Genet; 1985 Feb; 20(2):369-84. PubMed ID: 2579556 [TBL] [Abstract][Full Text] [Related]
18. Prenatal laboratory diagnosis of hereditary disorders. Amniocentesis and fibroblast tissue culture permit in utero diagnosis of hereditary metabolic disorders. Perl DP R I Med J; 1971 Oct; 54(10):509-12. PubMed ID: 4255433 [No Abstract] [Full Text] [Related]