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References cont. 5) Lanning, Robert W., and Charlotte A. Brown. “An Improved Methodology for the Detection of the Common Mutation in the FGFR3 Gene Responsible for Achondroplasia.” Department of Pediatrics, Carolinas Medical Center, Charlotte, NC. Aug. 3, 1997.
6) Moutou, Celine, Catherine Rongieres, Karima Bettahar-Lebugle Nathalie Gardes, Christophe Philippe, and Stephane Viville. “Preimplantation genetic diagnosis for achondroplasia: genetics and gynaecological limits and difficulties.” Human Reproduction. Mar. 200. Health Module, pg. 509.
7) Sobetzko, Diana, Suzanne Braga, Anna Rudeberg, Andrea Superti-Fura. “Achondroplasia with the FGFR3 1138 a (G380R) mutation in two sibs sharing a 4p haplotype derived from their unaffected father.” Journal of Medical Genetics. London: Dec. 2000. Vol.37, Iss. 12; pg 958.