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A Heiberg

Showing results (61-70 of 75) with videos related to

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Developmental Medicine and Child Neurology|March 1, 1996
Vision, cognition and developmental characteristics of girls and women with Rett syndromeS von Tetzchner, K H Jacobsen, L Smith, et al.
Community Dentistry and Oral Epidemiology|December 1, 1980
Myofascial pain dysfunction (MPD) syndrome in twinsA Heiberg, B Helöe, A N Heiberg, et al.
Psychotherapy and Psychosomatics|January 1, 1978
A presentation of short-term psychotherapy project at the Oslo University Psychiatric ClinicA A Dahl, C I Dahl, A Heiberg, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Identical mutation in 55% of the ATM alleles in 11 Norwegian AT families: evidence for a founder effectK Laake, M Telatar, G A Geitvik, et al.
Journal of Medical Genetics|June 17, 2003
Somatic mosaicism in neurofibromatosis 2: prevalence and risk of disease transmission to offspringA Moyhuddin, M E Baser, C Watson, et al.
American Journal of Medical Genetics|January 1, 1986
Second trimester prenatal diagnosis of the fragile XN Tommerup, P Aula, B Gustavii, et al.
Clinical and Experimental Immunology|June 16, 2004
The impact of an early truncating founder ATM mutation on immunoglobulins, specific antibodies and lymphocyte populations in ataxia-telangiectasia patients and their parentsA Stray-Pedersen, T Jónsson, A Heiberg, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 20, 1990
[Are prosecuted parents allowed the benefit of the doubt in cases of child abuse?]T Aakhus, F Brosstad, J Halse, et al.
Human Genetics|January 1, 1985
Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19J A Donald, S C Wallis, A Kessling, et al.
Atherosclerosis|September 1, 1984
The use of polymorphic DNA and protein markers for the third complement component for determining linkage of familial hypercholesterolaemiaS E Humphries, J A Donald, J J McFadden, et al.
Pageof 8

Showing results (61-70 of 75) with videos related to

Sort By:
Pageof 8
Developmental Medicine and Child Neurology|March 1, 1996
Vision, cognition and developmental characteristics of girls and women with Rett syndromeS von Tetzchner, K H Jacobsen, L Smith, et al.
Community Dentistry and Oral Epidemiology|December 1, 1980
Myofascial pain dysfunction (MPD) syndrome in twinsA Heiberg, B Helöe, A N Heiberg, et al.
Psychotherapy and Psychosomatics|January 1, 1978
A presentation of short-term psychotherapy project at the Oslo University Psychiatric ClinicA A Dahl, C I Dahl, A Heiberg, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Identical mutation in 55% of the ATM alleles in 11 Norwegian AT families: evidence for a founder effectK Laake, M Telatar, G A Geitvik, et al.
Journal of Medical Genetics|June 17, 2003
Somatic mosaicism in neurofibromatosis 2: prevalence and risk of disease transmission to offspringA Moyhuddin, M E Baser, C Watson, et al.
American Journal of Medical Genetics|January 1, 1986
Second trimester prenatal diagnosis of the fragile XN Tommerup, P Aula, B Gustavii, et al.
Clinical and Experimental Immunology|June 16, 2004
The impact of an early truncating founder ATM mutation on immunoglobulins, specific antibodies and lymphocyte populations in ataxia-telangiectasia patients and their parentsA Stray-Pedersen, T Jónsson, A Heiberg, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 20, 1990
[Are prosecuted parents allowed the benefit of the doubt in cases of child abuse?]T Aakhus, F Brosstad, J Halse, et al.
Human Genetics|January 1, 1985
Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19J A Donald, S C Wallis, A Kessling, et al.
Atherosclerosis|September 1, 1984
The use of polymorphic DNA and protein markers for the third complement component for determining linkage of familial hypercholesterolaemiaS E Humphries, J A Donald, J J McFadden, et al.
Pageof 8