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U Drugge

Showing results (11-20 of 19) with videos related to

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American Journal of Medical Genetics|February 1, 1991
Fragile X families in a northern Swedish county: a genealogical study of possibly affected individuals in the nineteenth centuryU Drugge, H K Blomquist, K H Gustavson, et al.
American Journal of Medical Genetics|May 1, 1988
Fragile X families in a northern Swedish county--a genealogical study demonstrating apparent paternal transmission from the 18th centuryG Holmgren, H K Blomquist, U Drugge, et al.
Journal of Medical Genetics|May 1, 1995
Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical studyU Drugge, M Holmberg, G Holmgren, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1990
Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variationM Kyllerman, L Forsgren, G Sanner, et al.
American Journal of Medical Genetics|April 1, 1992
Study of individuals possibly affected with the fragile X syndrome in a large Swedish family in the 18th to 20th centuriesU Drugge, G Holmgren, H K Blomquist, et al.
Journal of Medical Genetics|May 1, 1993
Familial amyloidotic polyneuropathy in Sweden: a pedigree analysisU Drugge, R Andersson, F Chizari, et al.
Clinical Genetics|January 1, 1992
Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequencesG Holmgren, S Bergström, U Drugge, et al.
Clinical Genetics|February 1, 1994
The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9qJ Wahlström, L Ozelius, P Kramer, et al.
Human Genetics|August 1, 1994
Geographical distribution of haplotypes in Swedish families with Huntington's diseaseE Almqvist, S Andrew, J Theilmann, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
American Journal of Medical Genetics|February 1, 1991
Fragile X families in a northern Swedish county: a genealogical study of possibly affected individuals in the nineteenth centuryU Drugge, H K Blomquist, K H Gustavson, et al.
American Journal of Medical Genetics|May 1, 1988
Fragile X families in a northern Swedish county--a genealogical study demonstrating apparent paternal transmission from the 18th centuryG Holmgren, H K Blomquist, U Drugge, et al.
Journal of Medical Genetics|May 1, 1995
Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical studyU Drugge, M Holmberg, G Holmgren, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1990
Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variationM Kyllerman, L Forsgren, G Sanner, et al.
American Journal of Medical Genetics|April 1, 1992
Study of individuals possibly affected with the fragile X syndrome in a large Swedish family in the 18th to 20th centuriesU Drugge, G Holmgren, H K Blomquist, et al.
Journal of Medical Genetics|May 1, 1993
Familial amyloidotic polyneuropathy in Sweden: a pedigree analysisU Drugge, R Andersson, F Chizari, et al.
Clinical Genetics|January 1, 1992
Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequencesG Holmgren, S Bergström, U Drugge, et al.
Clinical Genetics|February 1, 1994
The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9qJ Wahlström, L Ozelius, P Kramer, et al.
Human Genetics|August 1, 1994
Geographical distribution of haplotypes in Swedish families with Huntington's diseaseE Almqvist, S Andrew, J Theilmann, et al.
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