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B C Hamel

Showing results (51-60 of 129) with videos related to

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American Journal of Medical Genetics|May 20, 1999
Longitudinal changes in cognitive-behavioral levels in three children with FRAXEG S Fisch, N J Carpenter, R Simensen, et al.
Case Reports in Genetics|June 7, 2017
Freeman-Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan AfricaA M Ali, R M Mbwasi, G Kinabo, et al.
Genetic Counseling (Geneva, Switzerland)|January 5, 2001
Angelman syndrome in three adult patients with atypical presentation and severe neurological complicationsG J Van Buggenhout, M J Descheemaeker, P Thiry, et al.
European Journal of Pediatrics|June 1, 1996
Additional congenital defects in anorectal malformationsE A Hassink, P N Rieu, B C Hamel, et al.
Atherosclerosis|August 23, 1996
Prevalence of familial mild hyperhomocysteinemiaD G Franken, G H Boers, H J Blom, et al.
Human Molecular Genetics|March 1, 1994
Six novel mutations in the alpha-galactosidase A gene in families with Fabry diseaseJ K Ploos van Amstel, R P Jansen, J G de Jong, et al.
American Journal of Medical Genetics|June 1, 1993
Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spotsH G Brunner, T Hulsebos, P M Steijlen, et al.
Human Genetics|April 1, 1994
Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic familyF A Hol, M P Geurds, O Jensson, et al.
Neuropediatrics|December 1, 1996
Spinal muscular atrophy combined with congenital heart disease: a report of two casesW M Mulleners, C M van Ravenswaay, F J Gabreëls, et al.
American Journal of Medical Genetics|July 12, 1996
Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findingsB C Hamel, A P Smits, B J Otten, et al.
Pageof 13

Showing results (51-60 of 129) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics|May 20, 1999
Longitudinal changes in cognitive-behavioral levels in three children with FRAXEG S Fisch, N J Carpenter, R Simensen, et al.
Case Reports in Genetics|June 7, 2017
Freeman-Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan AfricaA M Ali, R M Mbwasi, G Kinabo, et al.
Genetic Counseling (Geneva, Switzerland)|January 5, 2001
Angelman syndrome in three adult patients with atypical presentation and severe neurological complicationsG J Van Buggenhout, M J Descheemaeker, P Thiry, et al.
European Journal of Pediatrics|June 1, 1996
Additional congenital defects in anorectal malformationsE A Hassink, P N Rieu, B C Hamel, et al.
Atherosclerosis|August 23, 1996
Prevalence of familial mild hyperhomocysteinemiaD G Franken, G H Boers, H J Blom, et al.
Human Molecular Genetics|March 1, 1994
Six novel mutations in the alpha-galactosidase A gene in families with Fabry diseaseJ K Ploos van Amstel, R P Jansen, J G de Jong, et al.
American Journal of Medical Genetics|June 1, 1993
Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spotsH G Brunner, T Hulsebos, P M Steijlen, et al.
Human Genetics|April 1, 1994
Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic familyF A Hol, M P Geurds, O Jensson, et al.
Neuropediatrics|December 1, 1996
Spinal muscular atrophy combined with congenital heart disease: a report of two casesW M Mulleners, C M van Ravenswaay, F J Gabreëls, et al.
American Journal of Medical Genetics|July 12, 1996
Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findingsB C Hamel, A P Smits, B J Otten, et al.
Pageof 13