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K Devriendt

Showing results (191-200 of 230) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1996
Isolation of cosmids corresponding to the chromosome breakpoints of a de novo autosomal translocation, t(6;19)(p21;q13.1), in a patient with multicystic renal dysplasiaP M Groenen, E Garcia, R Thoelen, et al.
Cancer Genetics and Cytogenetics|February 1, 1993
Loss of the Y-chromosome in a malignant Sertoli tumorM S Aly, P Dal Cin, P Moerman, et al.
Clinical Genetics|April 14, 2015
Clinical implementation of NIPT - technical and biological challengesP Brady, N Brison, K Van Den Bogaert, et al.
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Parenting, family contexts, and personality characteristics in youngsters with VCFSP Prinzie, A Swillen, B Maes, et al.
Blood|June 22, 2001
Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutationK Freson, K Devriendt, G Matthijs, et al.
Molecular Syndromology|August 3, 2012
Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of SkillsA Denayer, H Van Esch, T de Ravel, et al.
Human Genetics|August 15, 2000
Isolated supravalvular aortic stenosis: functional haploinsufficiency of the elastin gene as a result of nonsense-mediated decayZ Urbán, V V Michels, S N Thibodeau, et al.
Journal of Medical Genetics|December 24, 1998
1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysisS W Knight, T J Vulliamy, N S Heiss, et al.
Journal of Medical Genetics|July 9, 2009
Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangementsB I Dimitrov, T de Ravel, J Van Driessche, et al.
Journal of Dental Research|July 22, 2017
A Comprehensive Craniofacial Study of 22q11.2 Deletion SyndromeA Lewyllie, J Roosenboom, K Indencleef, et al.
Pageof 23

Showing results (191-200 of 230) with videos related to

Sort By:
Pageof 23
Cytogenetics and Cell Genetics|January 1, 1996
Isolation of cosmids corresponding to the chromosome breakpoints of a de novo autosomal translocation, t(6;19)(p21;q13.1), in a patient with multicystic renal dysplasiaP M Groenen, E Garcia, R Thoelen, et al.
Cancer Genetics and Cytogenetics|February 1, 1993
Loss of the Y-chromosome in a malignant Sertoli tumorM S Aly, P Dal Cin, P Moerman, et al.
Clinical Genetics|April 14, 2015
Clinical implementation of NIPT - technical and biological challengesP Brady, N Brison, K Van Den Bogaert, et al.
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Parenting, family contexts, and personality characteristics in youngsters with VCFSP Prinzie, A Swillen, B Maes, et al.
Blood|June 22, 2001
Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutationK Freson, K Devriendt, G Matthijs, et al.
Molecular Syndromology|August 3, 2012
Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of SkillsA Denayer, H Van Esch, T de Ravel, et al.
Human Genetics|August 15, 2000
Isolated supravalvular aortic stenosis: functional haploinsufficiency of the elastin gene as a result of nonsense-mediated decayZ Urbán, V V Michels, S N Thibodeau, et al.
Journal of Medical Genetics|December 24, 1998
1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysisS W Knight, T J Vulliamy, N S Heiss, et al.
Journal of Medical Genetics|July 9, 2009
Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangementsB I Dimitrov, T de Ravel, J Van Driessche, et al.
Journal of Dental Research|July 22, 2017
A Comprehensive Craniofacial Study of 22q11.2 Deletion SyndromeA Lewyllie, J Roosenboom, K Indencleef, et al.
Pageof 23