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5. Chorionic biopsy for prenatal diagnosis. An investigative study of 110 cases. Watters PA; Stewart L Med J Aust; 1986 Jan; 144(2):64-7. PubMed ID: 3941647 [TBL] [Abstract][Full Text] [Related]
6. First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency). Speiser PW; Laforgia N; Kato K; Pareira J; Khan R; Yang SY; Whorwood C; White PC; Elias S; Schriock E J Clin Endocrinol Metab; 1990 Apr; 70(4):838-48. PubMed ID: 1969421 [TBL] [Abstract][Full Text] [Related]
7. [Current status and trends of prenatal gene diagnosis]. Ren Z; Zeng Y Zhonghua Fu Chan Ke Za Zhi; 1997 Nov; 32(11):643-5. PubMed ID: 9639760 [No Abstract] [Full Text] [Related]
8. [Status of prenatal diagnosis using direct interventions on the fetus]. Weise W Zentralbl Gynakol; 1985; 107(15):913-28. PubMed ID: 3901609 [TBL] [Abstract][Full Text] [Related]
9. [Prenatal diagnosis of congenital diseases by chorionic villi sampling: an updated review]. Barkai G Harefuah; 1992 Dec; 123(11):502-5. PubMed ID: 1487214 [No Abstract] [Full Text] [Related]
10. [Prenatal molecular genetic diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency]. Rodríguez A; Ezquieta B; Varela JM; Moreno M; Dulín E; Rodríguez Arnao MD Med Clin (Barc); 1997 Nov; 109(17):669-72. PubMed ID: 9488957 [TBL] [Abstract][Full Text] [Related]
11. Fetal defects may be detectable in the first trimester with experimental biopsy technique. Fam Plann Perspect; 1983; 15(6):284-6. PubMed ID: 6667738 [No Abstract] [Full Text] [Related]
14. [Determination of fetal karyotype in the first trimester of pregnancy by direct examination of chorionic villi]. Flori E; Nisand I; Flori J; Spielmann A; Durand JL; Ruch JV; Dellenbach P J Genet Hum; 1985 Jun; 33(2):167-9. PubMed ID: 4020351 [TBL] [Abstract][Full Text] [Related]