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Journal Abstract Search
126 related items for PubMed ID: 153444
1. Prenatal diagnosis in New South Wales: comparative view of the first 1000 cases of chromosomal, sex-linked, and metabolic referrals. Daniel A, Lam-Po-Tang PR. Med J Aust; 1978 Oct 07; 2(8):352-7. PubMed ID: 153444 [Abstract] [Full Text] [Related]
2. Prenatal diagnosis in 3,000 women for chromosome, X-linked, and metabolic disorders. Daniel A, Stewart L, Saville T, Brookwell R, Paull H, Purvis-Smith S, Lam-Po-Tang PR. Am J Med Genet; 1982 Jan 07; 11(1):61-75. PubMed ID: 7065004 [Abstract] [Full Text] [Related]
3. European experience with prenatal diagnosis of congenital disease: a survey of 6121 cases. Galjaard H. Cytogenet Cell Genet; 1976 Jan 07; 16(6):453-67. PubMed ID: 789015 [Abstract] [Full Text] [Related]
4. [Prenatal diagnosis in 350 amniocenteses]. Grether P, Zavaleta MJ, de la Luna E, Sánchez-Solis V, Hernández C, Karchmer S. Ginecol Obstet Mex; 1991 Nov 07; 59():317-22. PubMed ID: 1797616 [Abstract] [Full Text] [Related]
5. Chromosomal abnormality rates at amniocentesis and in live-born infants. Hook EB, Cross PK, Schreinemachers DM. JAMA; 1983 Apr 15; 249(15):2034-8. PubMed ID: 6220164 [Abstract] [Full Text] [Related]
6. Age-specific incidences of chromosome abnormalities at the second trimester amniocentesis for Japanese mothers aged 35 and older: collaborative study of 5484 cases. Yaegashi N, Senoo M, Uehara S, Suzuki H, Maeda T, Fujimori K, Hirahara F, Yajima A. J Hum Genet; 1998 Apr 15; 43(2):85-90. PubMed ID: 9621511 [Abstract] [Full Text] [Related]
7. [Prenatal diagnosis. Review, personal and prospective studies]. Engel E, Empson J, DeLozier D, McGee B, da Costa Woodson E, Engel-de Montmollin M, Carter T, Lorber C, Cassidy SB, Millis J, Heller RM, Boehm F, Vanhooydonk J. Schweiz Med Wochenschr; 1979 Jul 07; 109(27):998-1010. PubMed ID: 88763 [Abstract] [Full Text] [Related]
9. Prenatal cytogenetic analysis of women with high risk for genetic disorders. Rary JM, Park IJ, Heller RH, Jones HW, Baramki TA. J Hered; 1974 Jul 07; 65(4):209-12. PubMed ID: 4278231 [Abstract] [Full Text] [Related]
11. [Value of detection of cell-free fetal DNA in maternal plasma in the prenatal diagnosis of chromosomal abnormalities]. Wang SJ, Gao ZY, Lu YP, Li YL, You YQ, Zhang LW, Wang LX, Xu H. Zhonghua Fu Chan Ke Za Zhi; 2012 Nov 07; 47(11):808-12. PubMed ID: 23302119 [Abstract] [Full Text] [Related]
12. Genetics, amniocentesis, and abortion. Hirschhorn K. Mt Sinai J Med; 1984 Nov 07; 51(1):15-7. PubMed ID: 6608672 [Abstract] [Full Text] [Related]
13. Amniocentesis for antenatal diagnosis. Elias S. Compr Ther; 1982 Jun 07; 8(6):21-5. PubMed ID: 6179702 [Abstract] [Full Text] [Related]
14. Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration. A European Collaborative Study on Prenatal Diagnoses 1981. Stene J, Stene E, Mikkelsen M. Prenat Diagn; 1984 Jun 07; 4 Spec No():81-95. PubMed ID: 6235486 [Abstract] [Full Text] [Related]
16. Prenatal diagnosis of chromosomal abnormalities: analysis of 1000 consecutive amniotic fluids. Bell JA, Ansford AJ. Aust N Z J Obstet Gynaecol; 1981 Nov 07; 21(4):207-10. PubMed ID: 6462129 [Abstract] [Full Text] [Related]
18. Screening for fetal chromosome aberrations in early pregnancy. Ferguson-Smith MA, Ferguson-Smith ME. J Clin Pathol Suppl (R Coll Pathol); 1976 Nov 07; 10():165-76. PubMed ID: 135003 [Abstract] [Full Text] [Related]
19. The antenatal detection of genetic disorders. Current status and future prospects. Golbus MS. Obstet Gynecol; 1976 Oct 07; 48(4):497-506. PubMed ID: 135214 [No Abstract] [Full Text] [Related]