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8. The clinical utility of fetal cell sorting to determine prenatally fetal E/e or e/e Rh genotype from peripheral maternal blood. Geifman-Holtzman O; Makhlouf F; Kaufman L; Gonchoroff NJ; Holtzman EJ Am J Obstet Gynecol; 2000 Aug; 183(2):462-8. PubMed ID: 10942488 [TBL] [Abstract][Full Text] [Related]
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10. In-cell PCR method for specific genotyping of genomic DNA from one individual in a mixture of cells from two individuals: a model study with specific relevance to prenatal diagnosis based on fetal cells in maternal blood. Hviid TV Clin Chem; 2002 Dec; 48(12):2115-23. PubMed ID: 12446466 [TBL] [Abstract][Full Text] [Related]
11. DNA typing of forensic material with mixed genotypes using allele-specific enzymatic amplification (polymerase chain reaction). Gyllensten UB; Josefsson A; Schemschat K; Saldeen T; Petterson U Forensic Sci Int; 1992 Jan; 52(2):149-60. PubMed ID: 1601347 [TBL] [Abstract][Full Text] [Related]
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13. [Association between HLA-DQA1, HLA-DQB1 alleles and risk of early pregnancy loss]. Sipak-Szmigiel O; Ronin-Walknowska E; Mikłaszewicz A; Dołubeczko A; Zejmo M; Giedrys-Kalemba S Ginekol Pol; 2007 Oct; 78(10):792-5. PubMed ID: 18200971 [TBL] [Abstract][Full Text] [Related]
14. Limited feasibility of routinely analyzing fetal cells from maternal blood by using magnetic activated cell sorting and polymerase chain reaction for prenatal diagnosis. Lin SK; Ho ES; Hsieh YT; Lo FC; Lai HY; Chen MH Zhonghua Yi Xue Za Zhi (Taipei); 2002 Dec; 65(12):594-9. PubMed ID: 12636205 [TBL] [Abstract][Full Text] [Related]
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16. Detection of paternally inherited fetal point mutations for β-thalassemia in maternal plasma using simple fetal DNA enrichment protocol with or without whole genome amplification: an accuracy assessment. Ramezanzadeh M; Salehi M; Farajzadegan Z; Kamali S; Salehi R J Matern Fetal Neonatal Med; 2016; 29(16):2645-9. PubMed ID: 26553322 [TBL] [Abstract][Full Text] [Related]
17. Distribution of HLA DQA.1 alleles in New Zealand Caucasian, Maori and Pacific Islander populations. Comparison with other population studies. Stringer P; Triggs CM; Baldwin LC; Melia LM; Savill MG Int J Legal Med; 1995; 108(1):2-7. PubMed ID: 7495681 [TBL] [Abstract][Full Text] [Related]
18. Molecular analysis and polymorphism of the DLA-DQA gene. Wagner JL; Burnett RC; DeRose SA; Storb R Tissue Antigens; 1996 Sep; 48(3):199-204. PubMed ID: 8896179 [TBL] [Abstract][Full Text] [Related]
19. Use of maternal plasma for non-invasive prenatal diagnosis of fetal ABO genotypes. Meng JL; Wang XT; Wang Y; Yue YF; Wang X; Chen ZJ Clin Chem Lab Med; 2007; 45(8):981-6. PubMed ID: 17867986 [TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of the fetal Rhc genotype from peripheral maternal blood. Geifman-Holtzman O; Kaufman L; Gonchoroff N; Bernstein I; Holtzman EJ Obstet Gynecol; 1998 Apr; 91(4):506-10. PubMed ID: 9540931 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]