Zobrazeno 1 - 5
of 5
pro vyhledávání: '"D D Koeberl"'
Publikováno v:
American journal of human genetics. 57(3)
The prognosis for 45,X/46,XX mosaicism diagnosed prenatally has yet to be established. We report our experience with 12 patients in whom prenatal diagnosis of 45,X/46,XX mosaicism was detected by amniocentesis for advanced maternal age or decreased m
Publikováno v:
American journal of human genetics. 47(2)
Spontaneous mutation provides the substrate for evolution on one hand and for genetic susceptibility to disease on the other hand. X-linked diseases such as hemophilia B offer an opportunity to examine recent germ-line mutations in humans. By utilizi
Autor:
D D Koeberl, B D Sun, T V Damodaran, T Brown, D S Millington, D K Benjamin, A Bird, A Schneider, S Hillman, M Jackson, R M Beaty, Y T Chen
Publikováno v:
Gene Therapy. 14:281-281
Autor:
Kishnani PS; Division of Medical Genetics, Duke University Medical Center, Durham, NC 27710, USA. kishn001@mc.duke.edu, Faulkner E, VanCamp S, Jackson M, Brown T, Boney A, Koeberl D, Chen YT
Publikováno v:
Veterinary pathology [Vet Pathol] 2001 Jan; Vol. 38 (1), pp. 83-91.
Autor:
Moisset PA; Unité de Recherche en Génétique Humaine, CHUL, Université Laval, Ste.-Foy, Quebec, Canada., Bonham L, Skuk D, Koeberl D, Brussee V, Goulet M, Roy B, Asselin I, Miller AD, Tremblay JP
Publikováno v:
Human gene therapy [Hum Gene Ther] 2000 Jun 10; Vol. 11 (9), pp. 1277-88.