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6. [Prenatal diagnosis: molecular basis and techniques used in the diagnosis of monogenic hereditary diseases]. Villegas Martínez A An Med Interna; 1989 May; 6(5):227-9. PubMed ID: 2577487 [No Abstract] [Full Text] [Related]
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9. Molecular approaches for screening of genetic diseases. Marian AJ Chest; 1995 Jul; 108(1):255-65. PubMed ID: 7606967 [No Abstract] [Full Text] [Related]
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11. Danger of delay for genetic tests. Newmark P Nature; 1986 Jun 5-11; 321(6070):557. PubMed ID: 3520337 [TBL] [Abstract][Full Text] [Related]
12. Prenatal exclusion of Norrie's disease. Redmond RM; Graham CA; Kelly ED; Coleman M; Nevin NC Br J Ophthalmol; 1992 Aug; 76(8):491-3. PubMed ID: 1390533 [TBL] [Abstract][Full Text] [Related]
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16. 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]
17. Prenatal diagnosis of genetic disorders. Henry G J Reprod Med; 1979 Oct; 23(4):185-93. PubMed ID: 390142 [No Abstract] [Full Text] [Related]
18. Noninvasive prenatal diagnosis using next-generation sequencing. Xu L; Shi R Gynecol Obstet Invest; 2014; 77(2):73-7. PubMed ID: 24192219 [TBL] [Abstract][Full Text] [Related]
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