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K Devriendt

Showing results (161-170 of 230) with videos related to

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European Journal of Medical Genetics|June 5, 2012
Sporadic male patients with intellectual disability: contribution of X-chromosome copy number variantsM Isrie, G Froyen, K Devriendt, et al.
Clinical Genetics|May 21, 2004
ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarismH Van Esch, K Poirier, F de Zegher, et al.
European Journal of Pediatrics|May 14, 1998
Vesico-ureteral reflux: a genetic condition?K Devriendt, P Groenen, H Van Esch, et al.
Acta Endocrinologica|April 1, 1993
Opposite effects of growth hormone and estrogens on the pregnancy zone protein serum levels in children and adolescentsK Devriendt, G Massa, F de Zegher, et al.
American Journal of Medical Genetics|January 8, 1999
Familial deletions of chromosome 22q11: the Leuven experienceA Swillen, K Devriendt, G Vantrappen, et al.
Annales De Genetique|July 18, 2002
The psychopathological phenotype of velo-cardio-facial syndromeA Vogels, W M A Verhoeven, S Tuinier, et al.
American Journal of Medical Genetics|September 12, 2000
Novel syndromic form of X-linked complicated spastic paraplegiaS Claes, K Devriendt, G Van Goethem, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experienceG Vantrappen, K Devriendt, A Swillen, et al.
Human Genetics|October 6, 1998
Missense mutation and hexanucleotide duplication in the PAX2 gene in two unrelated families with renal-coloboma syndrome (MIM 120330)K Devriendt, G Matthijs, B Van Damme, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Psychotic disorders in Prader-Willi syndromeA Vogels, M De Hert, M J Descheemaeker, et al.
Pageof 23

Showing results (161-170 of 230) with videos related to

Sort By:
Pageof 23
European Journal of Medical Genetics|June 5, 2012
Sporadic male patients with intellectual disability: contribution of X-chromosome copy number variantsM Isrie, G Froyen, K Devriendt, et al.
Clinical Genetics|May 21, 2004
ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarismH Van Esch, K Poirier, F de Zegher, et al.
European Journal of Pediatrics|May 14, 1998
Vesico-ureteral reflux: a genetic condition?K Devriendt, P Groenen, H Van Esch, et al.
Acta Endocrinologica|April 1, 1993
Opposite effects of growth hormone and estrogens on the pregnancy zone protein serum levels in children and adolescentsK Devriendt, G Massa, F de Zegher, et al.
American Journal of Medical Genetics|January 8, 1999
Familial deletions of chromosome 22q11: the Leuven experienceA Swillen, K Devriendt, G Vantrappen, et al.
Annales De Genetique|July 18, 2002
The psychopathological phenotype of velo-cardio-facial syndromeA Vogels, W M A Verhoeven, S Tuinier, et al.
American Journal of Medical Genetics|September 12, 2000
Novel syndromic form of X-linked complicated spastic paraplegiaS Claes, K Devriendt, G Van Goethem, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experienceG Vantrappen, K Devriendt, A Swillen, et al.
Human Genetics|October 6, 1998
Missense mutation and hexanucleotide duplication in the PAX2 gene in two unrelated families with renal-coloboma syndrome (MIM 120330)K Devriendt, G Matthijs, B Van Damme, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Psychotic disorders in Prader-Willi syndromeA Vogels, M De Hert, M J Descheemaeker, et al.
Pageof 23