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E Smeets

Showing results (11-20 of 59) with videos related to

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Helvetica Paediatrica Acta|October 1, 1987
Distal 11q deletion: a specific clinical entityJ P Fryns, A Kleczkowska, E Smeets, et al.
Annales De Genetique|January 1, 1992
Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her sonJ P Fryns, A Kleczkowska, E Smeets, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Noonan phenotype in the basal cell nevus syndromeC Grubben, J P Fryns, E Smeets, et al.
Annales De Genetique|February 16, 2000
Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosomeT Lukusa, L van den Berghe, E Smeets, et al.
Human Mutation|July 23, 2003
Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: implications for routine diagnosis of Rett syndromeE Schollen, E Smeets, E Deflem, et al.
Journal of Internal Medicine|October 1, 1991
Severe coagulopathy after a bite from a 'harmless' snake (Rhabdophis subminiatus)R E Smeets, P G Melman, J J Hoffmann, et al.
American Journal of Medical Genetics. Part A|June 1, 2011
Rett syndrome: a study of the faceJudith E Allanson, Raoul C M Hennekam, Ute Moog, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1979
Nervous system complications of herpes zoster: immunofluorescent demonstration of varicella-zoster antigen in CSF cellsA C Peters, J Versteeg, G T Bots, et al.
American Journal of Medical Genetics|February 5, 1998
De novo 7q36 deletion: breakpoint analysis and types of holoprosencephalyS G Frints, E F Schoenmakers, E Smeets, et al.
Clinical Genetics|June 1, 1988
The 49,XXXXY syndrome. Clinical and psychological follow-up dataM Borghgraef, J P Fryns, E Smeets, et al.
Pageof 6

Showing results (11-20 of 59) with videos related to

Sort By:
Pageof 6
Helvetica Paediatrica Acta|October 1, 1987
Distal 11q deletion: a specific clinical entityJ P Fryns, A Kleczkowska, E Smeets, et al.
Annales De Genetique|January 1, 1992
Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her sonJ P Fryns, A Kleczkowska, E Smeets, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Noonan phenotype in the basal cell nevus syndromeC Grubben, J P Fryns, E Smeets, et al.
Annales De Genetique|February 16, 2000
Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosomeT Lukusa, L van den Berghe, E Smeets, et al.
Human Mutation|July 23, 2003
Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: implications for routine diagnosis of Rett syndromeE Schollen, E Smeets, E Deflem, et al.
Journal of Internal Medicine|October 1, 1991
Severe coagulopathy after a bite from a 'harmless' snake (Rhabdophis subminiatus)R E Smeets, P G Melman, J J Hoffmann, et al.
American Journal of Medical Genetics. Part A|June 1, 2011
Rett syndrome: a study of the faceJudith E Allanson, Raoul C M Hennekam, Ute Moog, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1979
Nervous system complications of herpes zoster: immunofluorescent demonstration of varicella-zoster antigen in CSF cellsA C Peters, J Versteeg, G T Bots, et al.
American Journal of Medical Genetics|February 5, 1998
De novo 7q36 deletion: breakpoint analysis and types of holoprosencephalyS G Frints, E F Schoenmakers, E Smeets, et al.
Clinical Genetics|June 1, 1988
The 49,XXXXY syndrome. Clinical and psychological follow-up dataM Borghgraef, J P Fryns, E Smeets, et al.
Pageof 6