Author:
Brown W. T.,Gross A.,Chan C.,Jenkins E. C.,Mandel J. L.,Oberl� I.,Arveiler B.,Novelli G.,Thibodeau S.,Hagerman R.,Summers K.,Turner G.,White B. N.,Mulligan L.,Forster-Gibson C.,Holden J. J. A.,Zoll B.,Krawczak M.,Goonewardena P.,Gustavson K. H.,Pettersson U.,Holmgren G.,Schwartz C.,Howard-Peebles P. N.,Murphy P.,Breg W. R.,Veenema H.,Carpenter N. J.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference32 articles.
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3. Brown WT, Jenkins EC, Gross AC, Chan CB, Krawczun MS, Duncan CJ, Sklower SL, Fisch GS (1987a) Further evidence for genetic heterogeneity in the fragile X syndrome. Hum Genet 75:311?321
4. Brown WT, Wu Y, Gross AC, Chan CB, Dobkin CS, Jenkins EC (1987b) RFLP for linkage analysis of fragile X syndrome. Lancet I:280
5. Brown WT, Jenkins EC, Gross AC, Chan CB, Krawczun MS, Alonso ML, Cantu ES, Davis JG, Hagerman RJ, Laxova R, Liebowitz M, Penchaszadeh VB, Thibodeau S, Willey AM, Williamson MK, Willner JP, Zellers NJ (1988) Clinical use of DNa markers in the fragile (X) syndrome for carrier detection and prenatal diagnosis. In: Willey AM (ed) Nucleic acid probes in diagnosis of human genetic diseases. Liss, New York, pp 11?34
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