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5. The D1152H cystic fibrosis mutation in prenatal carrier screening, patients and prenatal diagnosis. Peleg L; Karpati M; Bronstein S; Berkenstadt M; Frydman M; Yonath H; Pras E J Med Screen; 2011; 18(4):169-72. PubMed ID: 22156145 [TBL] [Abstract][Full Text] [Related]
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20. Reduced allele dropout in single-cell analysis for preimplantation genetic diagnosis of cystic fibrosis. Ray PF; Winston RM; Handyside AH J Assist Reprod Genet; 1996 Feb; 13(2):104-6. PubMed ID: 8688580 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]