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S Hemmer

Showing results (21-30 of 48) with videos related to

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Human Molecular Genetics|December 1, 1994
Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosityM M Nöthen, S Cichon, S Hemmer, et al.
Cancer Genetics and Cytogenetics|February 25, 2000
DNA copy number losses at 1p32-pter in monozygotic twins concordant for breast cancerW el-Rifai, L Tarmo, S Hemmer, et al.
Biological Psychiatry|February 1, 1995
No association between length of the (CAG)n repeat of the Huntington's disease gene and Tourette's syndromeJ Hebebrand, M M Nöthen, B Klug, et al.
Der Orthopade|November 13, 2020
Bowel dysfunction after elective spinal surgery: etiology, diagnostics and management based on the medical literature and experience in a university hospitalA Jaber, S Hemmer, R Klotz, et al.
Der Orthopade|April 24, 2010
[Kyphectomy in myelomeningocele patients. Longterm results, complications and risk analysis]M Akbar, S Almatrod, C H Fürstenberg, et al.
Schizophrenia Research|May 1, 1996
Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial casesM Rietschel, M M Nöthen, M Albus, et al.
American Journal of Human Genetics|April 16, 1998
A gene for universal congenital alopecia maps to chromosome 8p21-22M M Nöthen, S Cichon, I R Vogt, et al.
The American Journal of Pathology|May 20, 1998
DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studiesS Knuutila, A M Björkqvist, K Autio, et al.
Molecular Psychiatry|March 24, 1999
Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German familiesM M Nöthen, S Cichon, H Rohleder, et al.
The American Journal of Pathology|September 17, 1999
DNA copy number losses in human neoplasmsS Knuutila, Y Aalto, K Autio, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|December 1, 1994
Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosityM M Nöthen, S Cichon, S Hemmer, et al.
Cancer Genetics and Cytogenetics|February 25, 2000
DNA copy number losses at 1p32-pter in monozygotic twins concordant for breast cancerW el-Rifai, L Tarmo, S Hemmer, et al.
Biological Psychiatry|February 1, 1995
No association between length of the (CAG)n repeat of the Huntington's disease gene and Tourette's syndromeJ Hebebrand, M M Nöthen, B Klug, et al.
Der Orthopade|November 13, 2020
Bowel dysfunction after elective spinal surgery: etiology, diagnostics and management based on the medical literature and experience in a university hospitalA Jaber, S Hemmer, R Klotz, et al.
Der Orthopade|April 24, 2010
[Kyphectomy in myelomeningocele patients. Longterm results, complications and risk analysis]M Akbar, S Almatrod, C H Fürstenberg, et al.
Schizophrenia Research|May 1, 1996
Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial casesM Rietschel, M M Nöthen, M Albus, et al.
American Journal of Human Genetics|April 16, 1998
A gene for universal congenital alopecia maps to chromosome 8p21-22M M Nöthen, S Cichon, I R Vogt, et al.
The American Journal of Pathology|May 20, 1998
DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studiesS Knuutila, A M Björkqvist, K Autio, et al.
Molecular Psychiatry|March 24, 1999
Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German familiesM M Nöthen, S Cichon, H Rohleder, et al.
The American Journal of Pathology|September 17, 1999
DNA copy number losses in human neoplasmsS Knuutila, Y Aalto, K Autio, et al.
Pageof 5