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C Hamel

Showing results (251-260 of 291) with videos related to

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Human Molecular Genetics|September 1, 1996
Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch familyH Kremer, L P Kuyt, B van den Helm, et al.
American Journal of Medical Genetics|July 9, 1999
X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3L E Siderius, B C Hamel, H van Bokhoven, et al.
American Journal of Medical Genetics|July 9, 1999
Down syndrome in a population of elderly mentally retarded patients: genetic-diagnostic survey and implications for medical careG J Van Buggenhout, J C Trommelen, A Schoenmaker, et al.
American Journal of Human Genetics|November 1, 1993
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)H G Brunner, H T Brüggenwirth, W Nillesen, et al.
American Journal of Human Genetics|November 1, 1994
Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular dataB C Hamel, A P Smits, E de Graaff, et al.
Systematic Reviews|October 25, 2020
Psychosocial and pharmacologic interventions for methamphetamine addiction: protocol for a scoping review of the literatureC Hamel, K Corace, M Hersi, et al.
Bioorganic & Medicinal Chemistry Letters|May 7, 1999
N-hydroxyurea and hydroxamic acid inhibitors of cyclooxygenase and 5-lipoxygenaseP J Connolly, S K Wetter, K N Beers, et al.
Brain : a Journal of Neurology|October 1, 1991
Myotonic dystrophy. Predictive value of normal results on clinical examinationH G Brunner, H J Smeets, W Nillesen, et al.
Research in Developmental Disabilities|November 27, 2009
Profiling Fragile X Syndrome in males: strengths and weaknesses in cognitive abilitiesM J W Van der Molen, M Huizinga, H M Huizenga, et al.
Annals of Neurology|October 1, 1992
Familial adult-onset muscular dystrophy with leukoencephalopathyB G van Engelen, Q H Leyten, P L Bernsen, et al.
Pageof 30

Showing results (251-260 of 291) with videos related to

Sort By:
Pageof 30
Human Molecular Genetics|September 1, 1996
Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch familyH Kremer, L P Kuyt, B van den Helm, et al.
American Journal of Medical Genetics|July 9, 1999
X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3L E Siderius, B C Hamel, H van Bokhoven, et al.
American Journal of Medical Genetics|July 9, 1999
Down syndrome in a population of elderly mentally retarded patients: genetic-diagnostic survey and implications for medical careG J Van Buggenhout, J C Trommelen, A Schoenmaker, et al.
American Journal of Human Genetics|November 1, 1993
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)H G Brunner, H T Brüggenwirth, W Nillesen, et al.
American Journal of Human Genetics|November 1, 1994
Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular dataB C Hamel, A P Smits, E de Graaff, et al.
Systematic Reviews|October 25, 2020
Psychosocial and pharmacologic interventions for methamphetamine addiction: protocol for a scoping review of the literatureC Hamel, K Corace, M Hersi, et al.
Bioorganic & Medicinal Chemistry Letters|May 7, 1999
N-hydroxyurea and hydroxamic acid inhibitors of cyclooxygenase and 5-lipoxygenaseP J Connolly, S K Wetter, K N Beers, et al.
Brain : a Journal of Neurology|October 1, 1991
Myotonic dystrophy. Predictive value of normal results on clinical examinationH G Brunner, H J Smeets, W Nillesen, et al.
Research in Developmental Disabilities|November 27, 2009
Profiling Fragile X Syndrome in males: strengths and weaknesses in cognitive abilitiesM J W Van der Molen, M Huizinga, H M Huizenga, et al.
Annals of Neurology|October 1, 1992
Familial adult-onset muscular dystrophy with leukoencephalopathyB G van Engelen, Q H Leyten, P L Bernsen, et al.
Pageof 30