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3. Detection of fetal DNA in maternal blood by PCR. Holzgreve W; Gänshirt-Ahlert D; Burschyk M; Horst J; Miny P; Gal A; Pohlschmidt M Lancet; 1990 May; 335(8699):1220-1. PubMed ID: 1971060 [No Abstract] [Full Text] [Related]
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5. DNA testing: diagnostic role in single gene conditions. Bodurtha J; Lloyd J; Tams L Va Med Q; 1992; 119(2):95-6. PubMed ID: 1562623 [No Abstract] [Full Text] [Related]
6. Progress in the genetic analysis of fetal cells circulating in maternal blood. Bianchi DW Curr Opin Obstet Gynecol; 1997 Apr; 9(2):121-5. PubMed ID: 9204234 [TBL] [Abstract][Full Text] [Related]
8. Amplification methods in the molecular diagnosis of genetic diseases. Ben-Ezra JM Clin Lab Med; 1995 Dec; 15(4):795-815. PubMed ID: 8838224 [TBL] [Abstract][Full Text] [Related]
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10. Strategies for the detection of autosomal fetal DNA sequence from maternal peripheral blood. Lo YM; Fleming KA; Wainscoat JS Ann N Y Acad Sci; 1994 Sep; 731():204-13. PubMed ID: 7524389 [No Abstract] [Full Text] [Related]
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13. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A. Kogan SC; Doherty M; Gitschier J N Engl J Med; 1987 Oct; 317(16):985-90. PubMed ID: 3657865 [TBL] [Abstract][Full Text] [Related]
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16. [The amplification of nucleotide sequences by PCR and the new technics for molecular diagnosis]. Goossens M Reprod Nutr Dev; 1990; Suppl 1():117s-124s. PubMed ID: 1698384 [TBL] [Abstract][Full Text] [Related]
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