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H Arnell

Showing results (1-10 of 10) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|June 26, 1998
The genetics of nocturnal enuresis: a simple question of complexityH Arnell
Human Genetics|September 1, 1997
Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21-q22H Arnell, A Nemeth, G Annerén, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 1, 1996
Growth and pubertal development in Down syndromeH Arnell, J Gustafsson, S A Ivarsson, et al.
Acta Ophthalmologica Scandinavica|January 9, 1999
Stargardt disease: linkage to the ABCR gene region on 1p21-p22 in Scandinavian familiesH Arnell, M Mäntyjärvi, K Tuppurainen, et al.
Muscle & Nerve|December 1, 1996
Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadismA Melberg, H Arnell, N Dahl, et al.
Journal of Medical Genetics|May 1, 1997
The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12qH Arnell, K Hjälmås, M Jägervall, et al.
European Heart Journal|July 1, 1996
Echocardiographic right and left ventricular measurements in male elite endurance athletesE Henriksen, J Landelius, L Wesslén, et al.
The American Journal of Cardiology|February 15, 1997
An echocardiographic study comparing male Swedish elite orienteers with other elite endurance athletesE Henriksen, J Landelius, L Wesslén, et al.
BMJ (Clinical Research Ed.)|January 22, 2000
Survey of unlicensed and off label drug use in paediatric wards in European countries. European Network for Drug Investigation in ChildrenS Conroy, I Choonara, P Impicciatore, et al.
Nature Genetics|November 7, 1998
A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasisS S Strautnieks, L N Bull, A S Knisely, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Acta Paediatrica (Oslo, Norway : 1992)|June 26, 1998
The genetics of nocturnal enuresis: a simple question of complexityH Arnell
Human Genetics|September 1, 1997
Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21-q22H Arnell, A Nemeth, G Annerén, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 1, 1996
Growth and pubertal development in Down syndromeH Arnell, J Gustafsson, S A Ivarsson, et al.
Acta Ophthalmologica Scandinavica|January 9, 1999
Stargardt disease: linkage to the ABCR gene region on 1p21-p22 in Scandinavian familiesH Arnell, M Mäntyjärvi, K Tuppurainen, et al.
Muscle & Nerve|December 1, 1996
Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadismA Melberg, H Arnell, N Dahl, et al.
Journal of Medical Genetics|May 1, 1997
The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12qH Arnell, K Hjälmås, M Jägervall, et al.
European Heart Journal|July 1, 1996
Echocardiographic right and left ventricular measurements in male elite endurance athletesE Henriksen, J Landelius, L Wesslén, et al.
The American Journal of Cardiology|February 15, 1997
An echocardiographic study comparing male Swedish elite orienteers with other elite endurance athletesE Henriksen, J Landelius, L Wesslén, et al.
BMJ (Clinical Research Ed.)|January 22, 2000
Survey of unlicensed and off label drug use in paediatric wards in European countries. European Network for Drug Investigation in ChildrenS Conroy, I Choonara, P Impicciatore, et al.
Nature Genetics|November 7, 1998
A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasisS S Strautnieks, L N Bull, A S Knisely, et al.
Pageof 1