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Wienker

Showing results (81-90 of 282) with videos related to

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Human Genetics|January 1, 1983
Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphismP Wieacker, N Horn, P Pearson, et al.
The American Journal of Cardiology|September 15, 1995
An angiotensin-converting enzyme gene variant is associated with acute myocardial infarction in women but not in menH Schuster, T F Wienker, U Stremmler, et al.
Biochemical Genetics|June 1, 1994
Biochemical genetics of methylglyoxal dehydrogenases in the laboratory rat (Rattus norvegicus)K Bender, R T Seibert, T F Wienker, et al.
Genetic Epidemiology|December 22, 1999
Linkage analysis with adequate modeling of a parent-of-origin effectK Strauch, R Fimmers, C Windemuth, et al.
Human Genetics|July 1, 1987
Linkage analysis with RFLPs in families with androgen resistance syndromes: evidence for close linkage between the androgen receptor locus and the DXS1 segmentP Wieacker, J E Griffin, T Wienker, et al.
Human Genetics|January 1, 1983
Linkage relationships between Retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosomeP Wieacker, T F Wienker, B Dallapiccola, et al.
European Archives of Psychiatry and Clinical Neuroscience|January 5, 2002
Towards the genetic basis of periodic catatonia: pedigree sample for genome scan I and IIG Stöber, B Pfuhlmann, G Nürnberg, et al.
Human Genetics|July 1, 1986
X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22M Mächler, D Frey, A Gal, et al.
Human Genetics|May 1, 1989
Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19M Koch, H Harley, M Sarfarazi, et al.
Human Genetics|January 1, 1985
X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal XqA Gal, J Mücke, H Theile, et al.
Pageof 29

Showing results (81-90 of 282) with videos related to

Sort By:
Pageof 29
Human Genetics|January 1, 1983
Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphismP Wieacker, N Horn, P Pearson, et al.
The American Journal of Cardiology|September 15, 1995
An angiotensin-converting enzyme gene variant is associated with acute myocardial infarction in women but not in menH Schuster, T F Wienker, U Stremmler, et al.
Biochemical Genetics|June 1, 1994
Biochemical genetics of methylglyoxal dehydrogenases in the laboratory rat (Rattus norvegicus)K Bender, R T Seibert, T F Wienker, et al.
Genetic Epidemiology|December 22, 1999
Linkage analysis with adequate modeling of a parent-of-origin effectK Strauch, R Fimmers, C Windemuth, et al.
Human Genetics|July 1, 1987
Linkage analysis with RFLPs in families with androgen resistance syndromes: evidence for close linkage between the androgen receptor locus and the DXS1 segmentP Wieacker, J E Griffin, T Wienker, et al.
Human Genetics|January 1, 1983
Linkage relationships between Retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosomeP Wieacker, T F Wienker, B Dallapiccola, et al.
European Archives of Psychiatry and Clinical Neuroscience|January 5, 2002
Towards the genetic basis of periodic catatonia: pedigree sample for genome scan I and IIG Stöber, B Pfuhlmann, G Nürnberg, et al.
Human Genetics|July 1, 1986
X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22M Mächler, D Frey, A Gal, et al.
Human Genetics|May 1, 1989
Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19M Koch, H Harley, M Sarfarazi, et al.
Human Genetics|January 1, 1985
X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal XqA Gal, J Mücke, H Theile, et al.
Pageof 29