Author:
Dahl N.,Hammarström-Heeroma K.,Goonewardena P.,Wadelius C.,Gustavson K. -H.,Holmgren G.,van Ommen G. J. B.,Pettersson U.
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference16 articles.
1. Arveiler B, Oberlé I, Vincent A, Hofker MH, Pearson PL, Mandel JL (1988) Genetic mapping of the Xq27?q28: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families. Am J Hum Genet 42:380?389
2. Brown TE, Wu Y, Gross AC, Chan BC, Dobkin CS, Jenkins EC (1987) RFLP for linkage analysis of fragile X syndrome (Letter). Lancet I:280
3. Brown WT, Gross A, Chan C, Jenkins EC, Mandel JL, Oberlé I, Arveiler I, Novelli G, Thibodeau S, Hagerman R, Summers K, Turner G, White BN, Mulligan L, Forster-Gibson C, Holden JJA, Zoll B, Krawczak M, Goonewardena P, Gustavson KH, Pettersson U, Holmgren G, Schwartz C, Howard-Peebles PN, Murphy P, Breg WR, Veneema H, Carpenter NJ (1988) Multilocus analysis of the fragile X syndrome. Hum Genet 78:201?205
4. Conneally PM, Edwards JH, Kidd KK, Lalouel J-M, Morton NE, Ott J, White R (1985) Report to the committee on methods of linkage analysis and reporting. Cytogenet Cell Genet 40:356?359
5. Cooper DN, Schmidtke J (1987) Diagnosis of genetic disease by recombinant DNA. Hum Genet 77:66?75
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