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The Journal of Biological Chemistry
|
October 5, 1990
A base substitution at a splice site in the COL3A1 gene causes exon skipping and generates abnormal type III procollagen in a patient with Ehlers-Danlos syndrome type IV
W G Cole, A A Chiodo, S R Lamande, et al.
American Journal of Human Genetics
|
July 27, 1999
Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993
S L White, V R Collins, R Wolfe, et al.
The Journal of Pediatrics
|
January 1, 1997
Mitochondrial myopathy with tRNA(Leu(UUR)) mutation and complex I deficiency responsive to riboflavin
R F Ogle, J Christodoulou, E Fagan, et al.
Annals of Neurology
|
March 1, 1996
Leigh syndrome: clinical features and biochemical and DNA abnormalities
S Rahman, R B Blok, H H Dahl, et al.
Surgical and Radiologic Anatomy : SRA
|
August 5, 2023
Combined cone-beam CT imaging and microsurgical dissection of cadaver specimens to study cerebral venous anatomy: a technical note
Markus E Krogager, Rasmus H Dahl, Lars Poulsgaard, et al.
The Journal of the Acoustical Society of America
|
September 1, 2022
Physical effects of sound exposure from underwater explosions on Pacific mackerel (Scomber japonicus): Effects on the inner ear
Michael E Smith, Alyssa W Accomando, Victoria Bowman, et al.
Journal of Medical Genetics
|
October 22, 2003
Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype
M G de Silva, K Elliott, H-H Dahl, et al.
The Journal of the Acoustical Society of America
|
May 4, 2020
Physical effects of sound exposure from underwater explosions on Pacific sardines (Sardinops sagax)
Peter H Dahl, A Keith Jenkins, Brandon Casper, et al.
Human Genetics
|
October 28, 1997
Molecular analysis of dihydropteridine reductase deficiency: identification of two novel mutations in Japanese patients
H Ikeda, Y Matsubara, H Mikami, et al.
Rhinology
|
March 16, 2026
uvenile nasopharyngeal angiofibroma: nationwide study on incidence, diagnosis, treatment, and recurrence
M El Haddouchi, P R G Eriksen, R H Dahl, et al.
Page
of 24
Search research articles
Search
Showing results (201-210 of 233) with videos related to
Sort By:
Page
of 24
The Journal of Biological Chemistry
|
October 5, 1990
A base substitution at a splice site in the COL3A1 gene causes exon skipping and generates abnormal type III procollagen in a patient with Ehlers-Danlos syndrome type IV
W G Cole, A A Chiodo, S R Lamande, et al.
American Journal of Human Genetics
|
July 27, 1999
Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993
S L White, V R Collins, R Wolfe, et al.
The Journal of Pediatrics
|
January 1, 1997
Mitochondrial myopathy with tRNA(Leu(UUR)) mutation and complex I deficiency responsive to riboflavin
R F Ogle, J Christodoulou, E Fagan, et al.
Annals of Neurology
|
March 1, 1996
Leigh syndrome: clinical features and biochemical and DNA abnormalities
S Rahman, R B Blok, H H Dahl, et al.
Surgical and Radiologic Anatomy : SRA
|
August 5, 2023
Combined cone-beam CT imaging and microsurgical dissection of cadaver specimens to study cerebral venous anatomy: a technical note
Markus E Krogager, Rasmus H Dahl, Lars Poulsgaard, et al.
The Journal of the Acoustical Society of America
|
September 1, 2022
Physical effects of sound exposure from underwater explosions on Pacific mackerel (Scomber japonicus): Effects on the inner ear
Michael E Smith, Alyssa W Accomando, Victoria Bowman, et al.
Journal of Medical Genetics
|
October 22, 2003
Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype
M G de Silva, K Elliott, H-H Dahl, et al.
The Journal of the Acoustical Society of America
|
May 4, 2020
Physical effects of sound exposure from underwater explosions on Pacific sardines (Sardinops sagax)
Peter H Dahl, A Keith Jenkins, Brandon Casper, et al.
Human Genetics
|
October 28, 1997
Molecular analysis of dihydropteridine reductase deficiency: identification of two novel mutations in Japanese patients
H Ikeda, Y Matsubara, H Mikami, et al.
Rhinology
|
March 16, 2026
uvenile nasopharyngeal angiofibroma: nationwide study on incidence, diagnosis, treatment, and recurrence
M El Haddouchi, P R G Eriksen, R H Dahl, et al.
Page
of 24