The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing.

Autor: Kunst, C B, Leeflang, E P, Iber, J C, Arnheim, N, Warren, S T

Publikováno v: Journal of Medical Genetics; Aug1997, Vol. 34 Issue 8, p627-631, 5p, 1 Black and White Photograph, 2 Charts, 1 Graph

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

Autor: Gunter C; Departments of Biochemistry, Pediatrics and Genetics, Emory University School of Medicine and Howard Hughes Medical Institute, Emory University, Atlanta, GA 30322, USA., Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, Schwartz C, Murray A, Macpherson JN, Sherman SL, Warren ST

Publikováno v: Human molecular genetics [Hum Mol Genet] 1998 Nov; Vol. 7 (12), pp. 1935-46.

FMR1 in global populations.

Autor: Kunst CB; Howard Hughes Medical Institute, Departments of Biochemistry and Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA., Zerylnick C, Karickhoff L, Eichler E, Bullard J, Chalifoux M, Holden JJ, Torroni A, Nelson DL, Warren ST

Publikováno v: American journal of human genetics [Am J Hum Genet] 1996 Mar; Vol. 58 (3), pp. 513-22.

Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes.

Autor: van den Ouweland AM; Department of Clinical Genetics, University Hospital, Rotterdam, The Netherlands., Deelen WH, Kunst CB, Uzielli ML, Nelson DL, Warren ST, Oostra BA, Halley DJ

Publikováno v: Human molecular genetics [Hum Mol Genet] 1994 Oct; Vol. 3 (10), pp. 1823-7.

Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28.

Autor: Gorlin JB; Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts., Henske E, Warren ST, Kunst CB, D'Urso M, Palmieri G, Hartwig JH, Bruns G, Kwiatkowski DJ

Publikováno v: Genomics [Genomics] 1993 Aug; Vol. 17 (2), pp. 496-8.