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Developmental Medicine and Child Neurology
|
March 1, 1996
Vision, cognition and developmental characteristics of girls and women with Rett syndrome
S von Tetzchner, K H Jacobsen, L Smith, et al.
Community Dentistry and Oral Epidemiology
|
December 1, 1980
Myofascial pain dysfunction (MPD) syndrome in twins
A 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 Clinic
A 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 effect
K 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 offspring
A Moyhuddin, M E Baser, C Watson, et al.
American Journal of Medical Genetics
|
January 1, 1986
Second trimester prenatal diagnosis of the fragile X
N 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 parents
A 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 19
J 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 hypercholesterolaemia
S E Humphries, J A Donald, J J McFadden, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 75) with videos related to
Sort By:
Page
of 8
Developmental Medicine and Child Neurology
|
March 1, 1996
Vision, cognition and developmental characteristics of girls and women with Rett syndrome
S von Tetzchner, K H Jacobsen, L Smith, et al.
Community Dentistry and Oral Epidemiology
|
December 1, 1980
Myofascial pain dysfunction (MPD) syndrome in twins
A 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 Clinic
A 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 effect
K 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 offspring
A Moyhuddin, M E Baser, C Watson, et al.
American Journal of Medical Genetics
|
January 1, 1986
Second trimester prenatal diagnosis of the fragile X
N 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 parents
A 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 19
J 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 hypercholesterolaemia
S E Humphries, J A Donald, J J McFadden, et al.
Page
of 8