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J Dissing

Showing results (21-30 of 29) with videos related to

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Annals of Human Genetics|March 30, 2000
Rapid and simple determination of hereditary haemochromatosis mutations by multiplex PCR-SSCP: detection of a new polymorphic mutationK Simonsen, J Dissing, L Rudbeck, et al.
Biochemical and Biophysical Research Communications|October 15, 1993
Exon structure at the human ACP1 locus supports alternative splicing model for f and s isozyme generationK D Lazaruk, J Dissing, G F Sensabaugh
Annals of Human Genetics|March 14, 2001
Human 18 kDa phosphotyrosine protein phosphatase (ACP1) polymorphism: studies of rare variants provide evidence that substitutions within or near alternatively spliced exons affect splicing resultL Rudbeck, J Dissing, K D Lazaruk, et al.
Human Genetics|May 1, 1987
Hydatidiform mole: genetic origin in polyploid conceptusesL O Vejerslev, J Dissing, H E Hansen, et al.
Cancer Genetics and Cytogenetics|May 1, 1987
Hydatidiform mole: genetic markers in diploid abortuses with macroscopic villous enlargementL O Vejerslev, J Dissing, H E Hansen, et al.
Hormone Research|January 1, 1982
Heterozygotes and cryptic patients in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency). HLA and glyoxalase I typing and hormonal studiesK E Petersen, A Svejgaard, M D Nielsen, et al.
Human Genetics|January 1, 1980
A linkage study of hereditary ataxias and related disorders. Evidence of heterogeneity of dominant cerebellar ataxiaL Pedersen, P Platz, L P Ryder, et al.
American Journal of Physical Anthropology|November 30, 2007
Rare mtDNA haplogroups and genetic differences in rich and poor Danish Iron-Age villagesL Melchior, M T P Gilbert, T Kivisild, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|January 7, 2003
HFE mutations and hemochromatosis in Danish patients admitted for HFE genotypingP Koefoed, K Dalhoff, J Dissing, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Annals of Human Genetics|March 30, 2000
Rapid and simple determination of hereditary haemochromatosis mutations by multiplex PCR-SSCP: detection of a new polymorphic mutationK Simonsen, J Dissing, L Rudbeck, et al.
Biochemical and Biophysical Research Communications|October 15, 1993
Exon structure at the human ACP1 locus supports alternative splicing model for f and s isozyme generationK D Lazaruk, J Dissing, G F Sensabaugh
Annals of Human Genetics|March 14, 2001
Human 18 kDa phosphotyrosine protein phosphatase (ACP1) polymorphism: studies of rare variants provide evidence that substitutions within or near alternatively spliced exons affect splicing resultL Rudbeck, J Dissing, K D Lazaruk, et al.
Human Genetics|May 1, 1987
Hydatidiform mole: genetic origin in polyploid conceptusesL O Vejerslev, J Dissing, H E Hansen, et al.
Cancer Genetics and Cytogenetics|May 1, 1987
Hydatidiform mole: genetic markers in diploid abortuses with macroscopic villous enlargementL O Vejerslev, J Dissing, H E Hansen, et al.
Hormone Research|January 1, 1982
Heterozygotes and cryptic patients in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency). HLA and glyoxalase I typing and hormonal studiesK E Petersen, A Svejgaard, M D Nielsen, et al.
Human Genetics|January 1, 1980
A linkage study of hereditary ataxias and related disorders. Evidence of heterogeneity of dominant cerebellar ataxiaL Pedersen, P Platz, L P Ryder, et al.
American Journal of Physical Anthropology|November 30, 2007
Rare mtDNA haplogroups and genetic differences in rich and poor Danish Iron-Age villagesL Melchior, M T P Gilbert, T Kivisild, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|January 7, 2003
HFE mutations and hemochromatosis in Danish patients admitted for HFE genotypingP Koefoed, K Dalhoff, J Dissing, et al.
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