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Clinical Genetics|December 1, 1987
Gamma-glutamyl transferase activity in the amniotic fluid of fetuses with chromosomal aberrations and inborn errors of metabolismM Macek, G Annerén, K H Gustavson, et al.Clinical Genetics|February 1, 1985
Frequency of the fragile X syndrome in infantile autism. A Swedish multicenter studyH K Blomquist, M Bohman, S O Edvinsson, et al.Southern Medical Journal|April 1, 1994
Birth defects surveillance: Jefferson County, Alabama, and Uppsala County, SwedenW H Finley, K H Gustavson, T M Hall, et al.Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1995
Severe mental retardation in 2 to 24-month-old children in Lahore, Pakistan: a prospective cohort studyM Yaqoob, A Bashir, K Tareen, et al.Clinical Genetics|September 1, 1992
The gene for Best's macular dystrophy is located at 11q13 in a Swedish familyK Forsman, C Graff, S Nordström, et al.American Journal of Human Genetics|July 1, 1995
Fine mapping of the congenital chloride diarrhea gene by linkage disequilibriumP Höglund, P Sistonen, R Norio, et al.American Journal of Human Genetics|August 1, 1989
Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304)N Dahl, P Goonewardena, H Malmgren, et al.American Journal of Human Genetics|June 1, 1993
Linkage mapping of a severe X-linked mental retardation syndromeH Malmgren, M Sundvall, N Dahl, et al.Human Genetics|June 1, 1989
Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndromeN Dahl, K Hammarström-Heeroma, P Goonewardena, et al.Journal of the Neurological Sciences|December 1, 1995
Autosomal dominant cerebellar ataxia deafness and narcolepsyA Melberg, J Hetta, N Dahl, et al.Pageof 14