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C Hamel

Showing results (231-240 of 291) with videos related to

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The New England Journal of Medicine|March 19, 1992
Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15D F Smeets, B C Hamel, M R Nelen, et al.
Journal of Medical Genetics|May 19, 2001
The small patella syndrome: description of five cases from three families and examination of possible allelism with familial patella aplasia-hypoplasia and nail-patella syndromeE M Bongers, H Van Bokhoven, M N Van Thienen, et al.
Journal of Medical Genetics|May 9, 2006
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%A-F Roux, V Faugère, S Le Guédard, et al.
Plos One|February 9, 2022
Economic evaluation of a randomized controlled trial comparing mifepristone and misoprostol with misoprostol alone in the treatment of early pregnancy lossCharlotte C Hamel, Marcus P L M Snijders, Sjors F P J Coppus, et al.
Bioorganic & Medicinal Chemistry Letters|November 19, 2003
Synthesis and biological evaluation of benzazepine oxazolidinone antibacterialsPaul D Johnson, Paul A Aristoff, Gary E Zurenko, et al.
Antimicrobial Agents and Chemotherapy|June 1, 1996
In vivo activities of U-100592 and U-100766, novel oxazolidinone antimicrobial agents, against experimental bacterial infectionsC W Ford, J C Hamel, D M Wilson, et al.
Journal of Medical Genetics|March 1, 1995
Absence of linkage between familial neural tube defects and PAX3 geneS Chatkupt, F A Hol, Y Y Shugart, et al.
Neuromuscular Disorders : NMD|September 1, 1994
The gene for X-linked myotubular myopathy is located in an 8 Mb region at the border of Xq27.3 and Xq28E A Janssen, G W Hensels, B A van Oost, et al.
Clinical Genetics|June 4, 1998
Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defectsF A Hol, N M van der Put, M P Geurds, et al.
Journal of Medical Genetics|August 1, 1996
PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifidaF A Hol, M P Geurds, S Chatkupt, et al.
Pageof 30

Showing results (231-240 of 291) with videos related to

Sort By:
Pageof 30
The New England Journal of Medicine|March 19, 1992
Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15D F Smeets, B C Hamel, M R Nelen, et al.
Journal of Medical Genetics|May 19, 2001
The small patella syndrome: description of five cases from three families and examination of possible allelism with familial patella aplasia-hypoplasia and nail-patella syndromeE M Bongers, H Van Bokhoven, M N Van Thienen, et al.
Journal of Medical Genetics|May 9, 2006
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%A-F Roux, V Faugère, S Le Guédard, et al.
Plos One|February 9, 2022
Economic evaluation of a randomized controlled trial comparing mifepristone and misoprostol with misoprostol alone in the treatment of early pregnancy lossCharlotte C Hamel, Marcus P L M Snijders, Sjors F P J Coppus, et al.
Bioorganic & Medicinal Chemistry Letters|November 19, 2003
Synthesis and biological evaluation of benzazepine oxazolidinone antibacterialsPaul D Johnson, Paul A Aristoff, Gary E Zurenko, et al.
Antimicrobial Agents and Chemotherapy|June 1, 1996
In vivo activities of U-100592 and U-100766, novel oxazolidinone antimicrobial agents, against experimental bacterial infectionsC W Ford, J C Hamel, D M Wilson, et al.
Journal of Medical Genetics|March 1, 1995
Absence of linkage between familial neural tube defects and PAX3 geneS Chatkupt, F A Hol, Y Y Shugart, et al.
Neuromuscular Disorders : NMD|September 1, 1994
The gene for X-linked myotubular myopathy is located in an 8 Mb region at the border of Xq27.3 and Xq28E A Janssen, G W Hensels, B A van Oost, et al.
Clinical Genetics|June 4, 1998
Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defectsF A Hol, N M van der Put, M P Geurds, et al.
Journal of Medical Genetics|August 1, 1996
PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifidaF A Hol, M P Geurds, S Chatkupt, et al.
Pageof 30