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Clinical genetics

Showing results (681-690 of 7,173) with videos related to

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Clinical Genetics|January 6, 2011
Clinical findings in patients with GLI2 mutations--phenotypic variabilityC D P Bertolacini, L A Ribeiro-Bicudo, A Petrin, et al.
Clinical Genetics|January 6, 2011
Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletionsM H Willemsen, G Beunders, M Callaghan, et al.
Clinical Genetics|January 6, 2011
Adoption and the communication of genetic risk: experiences in Huntington diseaseY Bombard, A Semaka, M R Hayden
Clinical Genetics|February 22, 2011
Critical appraisal of the revised Ghent criteria for diagnosis of Marfan syndromeT Radonic, P de Witte, M Groenink, et al.
Clinical Genetics|February 22, 2011
Functional characterization of the TSC2 c.3598C>T (p.R1200W) missense mutation that co-segregates with tuberous sclerosis complex in mildly affected kindredsM Wentink, M Nellist, M Hoogeveen-Westerveld, et al.
Clinical Genetics|October 2, 2009
Recent advances of genetic ancestry testing in biomedical research and direct to consumer testingM Via, E Ziv, E G Burchard
Clinical Genetics|October 2, 2009
Highly variable clinical phenotype of carbamylphosphate synthetase 1 deficiency in one family: an effect of allelic variation in gene expression?V Klaus, T Vermeulen, B Minassian, et al.
Clinical Genetics|October 2, 2009
Cornelia de Lange syndrome, cohesin, and beyondJ Liu, I D Krantz
Clinical Genetics|October 2, 2009
Hereditary hair loss and the ancient signaling pathways that regulate ectodermal appendage formationC D Van Raamsdonk
Clinical Genetics|October 2, 2009
Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literatureC Nemos, L Lambert, F Giuliano, et al.
Pageof 718

Showing results (681-690 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|January 6, 2011
Clinical findings in patients with GLI2 mutations--phenotypic variabilityC D P Bertolacini, L A Ribeiro-Bicudo, A Petrin, et al.
Clinical Genetics|January 6, 2011
Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletionsM H Willemsen, G Beunders, M Callaghan, et al.
Clinical Genetics|January 6, 2011
Adoption and the communication of genetic risk: experiences in Huntington diseaseY Bombard, A Semaka, M R Hayden
Clinical Genetics|February 22, 2011
Critical appraisal of the revised Ghent criteria for diagnosis of Marfan syndromeT Radonic, P de Witte, M Groenink, et al.
Clinical Genetics|February 22, 2011
Functional characterization of the TSC2 c.3598C>T (p.R1200W) missense mutation that co-segregates with tuberous sclerosis complex in mildly affected kindredsM Wentink, M Nellist, M Hoogeveen-Westerveld, et al.
Clinical Genetics|October 2, 2009
Recent advances of genetic ancestry testing in biomedical research and direct to consumer testingM Via, E Ziv, E G Burchard
Clinical Genetics|October 2, 2009
Highly variable clinical phenotype of carbamylphosphate synthetase 1 deficiency in one family: an effect of allelic variation in gene expression?V Klaus, T Vermeulen, B Minassian, et al.
Clinical Genetics|October 2, 2009
Cornelia de Lange syndrome, cohesin, and beyondJ Liu, I D Krantz
Clinical Genetics|October 2, 2009
Hereditary hair loss and the ancient signaling pathways that regulate ectodermal appendage formationC D Van Raamsdonk
Clinical Genetics|October 2, 2009
Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literatureC Nemos, L Lambert, F Giuliano, et al.
Pageof 718