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C Hamel

Showing results (241-250 of 291) with videos related to

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Human Immunology|February 26, 2000
Immunological tolerance in an HLA non-identical chimeric twinH E Viëtor, B C Hamel, S P van Bree, et al.
American Journal of Human Genetics|February 1, 1993
Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspectsR C Hennekam, M Tilanus, B C Hamel, et al.
Genomics|October 14, 2000
Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genesF A Hol, M T Schepens, S E van Beersum, et al.
Military Medicine|March 5, 2002
Nucleic acid molecular biomarkers for diagnostic biodosimetry applications: use of the fluorogenic 5'-nuclease polymerase chain reaction assayWilliam F Blakely, Alexandra C Miller, Lei Luo, et al.
Journal of Medical Genetics|October 23, 1998
Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26H G Yntema, B C Hamel, A P Smits, et al.
Journal of Neurophysiology|March 24, 2012
TRPV4 channels mediate the infrared laser-evoked response in sensory neuronsE S Albert, J M Bec, G Desmadryl, et al.
Neuromuscular Disorders : NMD|September 27, 2008
Clinical and molecular overlap between myopathies and inherited connective tissue diseasesN C Voermans, C G Bönnemann, P A Huijing, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Fountain syndrome: further delineation of the clinical syndrome and follow-up dataG J Van Buggenhout, C M Van Ravenswaaij-Arts, W O Renier, et al.
European Journal of Pediatrics|May 2, 2000
Maternal uniparental disomy 7--review and further delineation of the phenotypeD Kotzot, D Balmer, A Baumer, et al.
Teratology|October 19, 1999
Nonsyndromic orofacial clefts: association with maternal hyperhomocysteinemiaW Y Wong, T K Eskes, A M Kuijpers-Jagtman, et al.
Pageof 30

Showing results (241-250 of 291) with videos related to

Sort By:
Pageof 30
Human Immunology|February 26, 2000
Immunological tolerance in an HLA non-identical chimeric twinH E Viëtor, B C Hamel, S P van Bree, et al.
American Journal of Human Genetics|February 1, 1993
Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspectsR C Hennekam, M Tilanus, B C Hamel, et al.
Genomics|October 14, 2000
Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genesF A Hol, M T Schepens, S E van Beersum, et al.
Military Medicine|March 5, 2002
Nucleic acid molecular biomarkers for diagnostic biodosimetry applications: use of the fluorogenic 5'-nuclease polymerase chain reaction assayWilliam F Blakely, Alexandra C Miller, Lei Luo, et al.
Journal of Medical Genetics|October 23, 1998
Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26H G Yntema, B C Hamel, A P Smits, et al.
Journal of Neurophysiology|March 24, 2012
TRPV4 channels mediate the infrared laser-evoked response in sensory neuronsE S Albert, J M Bec, G Desmadryl, et al.
Neuromuscular Disorders : NMD|September 27, 2008
Clinical and molecular overlap between myopathies and inherited connective tissue diseasesN C Voermans, C G Bönnemann, P A Huijing, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Fountain syndrome: further delineation of the clinical syndrome and follow-up dataG J Van Buggenhout, C M Van Ravenswaaij-Arts, W O Renier, et al.
European Journal of Pediatrics|May 2, 2000
Maternal uniparental disomy 7--review and further delineation of the phenotypeD Kotzot, D Balmer, A Baumer, et al.
Teratology|October 19, 1999
Nonsyndromic orofacial clefts: association with maternal hyperhomocysteinemiaW Y Wong, T K Eskes, A M Kuijpers-Jagtman, et al.
Pageof 30