These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. Prenatal diagnosis with use of fetal cells isolated from maternal blood: five-color fluorescent in situ hybridization analysis on flow-sorted cells for chromosomes X, Y, 13, 18, and 21. Bischoff FZ; Lewis DE; Nguyen DD; Murrell S; Schober W; Scott J; Simpson JL; Elias S Am J Obstet Gynecol; 1998 Jul; 179(1):203-9. PubMed ID: 9704788 [TBL] [Abstract][Full Text] [Related]
24. Prenatal diagnosis of fetal lymphocytes in the maternal blood. Schindler AM; Martin-du-Pan R Obstet Gynecol; 1972 Sep; 40(3):340-6. PubMed ID: 5054963 [No Abstract] [Full Text] [Related]
25. Abnormal chromosome 18 in prenatal diagnosis with holoprosencephaly. de Pater JM; Scheres JM; Brons J Prenat Diagn; 1997 Sep; 17(9):887-8. PubMed ID: 9316141 [No Abstract] [Full Text] [Related]
26. [Prenatal diagnosis of congenital diseases of metabolism and of chromosomes alterations]. Saggese R Pediatria (Napoli); 1979 Dec; 87(4):631-47. PubMed ID: 400008 [No Abstract] [Full Text] [Related]
28. Will ultrasound-screening and ultrasound-guided procedures be replaced by non-invasive techniques for the diagnosis of fetal chromosome anomalies? Holzgreve W Ultrasound Obstet Gynecol; 1997 Apr; 9(4):217-9. PubMed ID: 9168569 [No Abstract] [Full Text] [Related]
29. [Ways to improve prenatal diagnosis of chromosome abnormalities and congenital defects of fetal development]. Bakharev VA; Polesterov IuA; Gavrilova IuV Akush Ginekol (Mosk); 1990 Jan; (1):16-8. PubMed ID: 1693812 [No Abstract] [Full Text] [Related]
30. [Prenatal diagnosis of chromosomal aberrations in first trimester pregnancy--methods for cytogenetic analysis of the trophoblast]. Jakubów K; Bocian E Ginekol Pol; 1993 Apr; 64(4):204-9. PubMed ID: 8282244 [TBL] [Abstract][Full Text] [Related]
31. Confirmation of the chromosome 8p23.1 euchromatic duplication as a variant with no clinical manifestations. O'Malley DP; Storto PD Prenat Diagn; 1999 Feb; 19(2):183-4. PubMed ID: 10215083 [No Abstract] [Full Text] [Related]
32. Rapid DNA quantification in the prenatal diagnosis of fetal triploidy. Thilaganathan B; Makrydimas G; Nicolaides KH Br J Obstet Gynaecol; 1993 Jan; 100(1):92-3. PubMed ID: 8427846 [No Abstract] [Full Text] [Related]
33. Abnormal facial features and extremities in human trisomy syndromes: prenatal US appearance. Benacerraf BR; Frigoletto FD; Greene MF Radiology; 1986 Apr; 159(1):243-6. PubMed ID: 3513249 [TBL] [Abstract][Full Text] [Related]
34. The roles of ultrasonography and amniocentesis in evaluation of elevated maternal serum alpha-fetoprotein. Lindfors KK; Gorczyca DP; Hanson FW; Tennant FR; McGahan JP; Peterson AG Am J Obstet Gynecol; 1991 Jun; 164(6 Pt 1):1571-5; discussion 1575-6. PubMed ID: 1710874 [TBL] [Abstract][Full Text] [Related]
35. Prenatal diagnosis of a congenital anomaly of isochromosome 18q--a case report. Shyu SK; Yang ML; Ng HT; Hsu I; Wang JS; Ho DM Zhonghua Yi Xue Za Zhi (Taipei); 1988 May; 41(5):383-8. PubMed ID: 3219651 [No Abstract] [Full Text] [Related]