Barker D, Wright E, Nguyen K, Cannon L, Fain P, Goldgar D, Bishop DT, Carey J, Baty B, Kivlin J, Willard H, Waye JS, Greig G, Leinwand L, Nakamura Y, O'Connell P, Leppert M, Lalouel J-M, White R, Skolnick M (1987) Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17. Science 236:1100–1102
Google Scholar
Barker DF, Fain PR, Wright EC, Nguyen K, Tsui LC (1989) MspI RFLP at CRYB1 locus (17q11. 2-17q12). Nucleic Acids Res 17:827
Google Scholar
Camera G, Mastroiacovo P (1982) Birth prevalence of skeletal dysplasias in the Italian Multicentric Monitoring System for Birth Defects. In: Papadatos CJ, Bartsocas CS (eds) Skeletal dysplasias. Liss, New York, pp 441–449
Google Scholar
Edwards JH, Huson S, Ponder B (1988) Neurofibromatosis. Lancet 11:330
Google Scholar
Fain PR, Barker DF, Goldgar DE, Wright E, Nguyen K, Johnson CJ, Kivlin J, Willard H, Mathew C, et al (1987) Genetic analysis of NF1:identification of close flanking markers on chromosome 17. Genomics 4:340–345
Google Scholar
Fain PR, Goldgar DE, Wallace MR, Collins FS, Wright E, Nguyen K, Barker DF (1989) Refined physical and genetic mapping of the NF1 region on chromosome 17. Am Hum Genet 45:721–728
Google Scholar
Feinberg A, Vogelstein B (1984) A technique for radiolabeling DNA restriction nuclease fragments to high specific activity. Anal Biochem 137:266–267
Google Scholar
Gardener RJM (1977) A new estimate of the achondroplasia mutation rate. Clin Genet 11:31–38
Google Scholar
Goldgar DE, Green P, Parry DM, Mulvihill JJ (1989) Multipoint linkage analysis in neurofibromatosis type I: an international collaboration. Am J Hum Gen 44:6–12
Google Scholar
Lathrop GM, Lalouel JM, Julier C, Ott J (1984) Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci USA 81:3443–3446
Google Scholar
Lathrop GM, Lalouel JM, Julier C, Ott J (1985) Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet 37:482–498
Google Scholar
Ogilvie D, Wardswarth P, Thompson E, Sykes B (1986) Evidence against the structural gene encoding type II collagen (COL2A1) as the mutant locus in achondroplasia. J Med Genet 23:19–22
Google Scholar
Orioli IM, Castilla EE, Barbosa-Neto JE (1986) The birth prevelance rates for skeletal dysplasias. J Med Genet 23:328–332
Google Scholar
Seizinger BR, Rouleau GA, Ozelius LJ, Lane AH, Faryniarz AG, Chao MV, Huson S, Korf BR, Parry DM, Pericak-Vance MA, Collins FS, Hobbs WJ, Falcone BG, Lannazzi JA, Roy JC, St George-Hyslop PH, Tanzi RE, Bothwell MA, Upadhyaya M, Harper P, Goldstein AE, Hoover DL, Bader JL, Spence MA, Mulvihill JJ, Aylsworth AS, Vance JM, Rossenwasser G, Gaskell PC, Roses AD, Martuza RL, Breakefield XO, Gusella JF (1987) Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene. Cell 49:589–594
Google Scholar
Wasman ER, Kovacks B, Rimoin DL, Sparkes R, Alfi O (1988) Achondroplasia, neurofibromatosis, and 47,XYY as new mutational events in a single individual. Am J Med Genet 43:[suppl]:A99
Google Scholar
White R, Nakamura Y, O'Connell P, Leppert M, Lalouel JM, Barker D, Goldgar D, Skolnick M, Carey J, Wallis CE, Slater CP, Mathew C, Ponder B (1987) Tightly linked markers for the neurofibromatosis type 1 gene. Genomics 1:364–367
Google Scholar
Willard HF, Waye JS, Skolnick MH, Schwartz CE, Powers VE, England SB (1986) Detection of restriction fragment polymorphisms at the centromeres of human chromosomes by using chromosome-specific satellite DNA probes; implications for development of centromere-based genetic linkage maps. Proc Natl Acad Sci USA 83:5611–5615
Google Scholar