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K Devriendt

Showing results (181-190 of 230) with videos related to

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B-ENT|November 26, 2015
Review: Facial endophenotypes in non-syndromic orofacial cleftingJ Roosenboom, P Claes, K Devriendt, et al.
Annales De Genetique|February 13, 2001
Cryptic translocation t(5;18) in familial mental retardationA Vogels, K Devriendt, J R Vermeesch, et al.
Clinical Genetics|April 1, 1997
Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletionK Devriendt, R Van Hoestenberghe, C Van Hole, et al.
American Journal of Human Genetics|March 1, 1997
Skewed X-chromosome inactivation in female carriers of dyskeratosis congenitaK Devriendt, G Matthijs, E Legius, et al.
Cytogenetic and Genome Research|November 25, 2006
Molecular karyotyping of patients with MCA/MR: the blurred boundary between normal and pathogenic variationT J L de Ravel, I Balikova, B Thienpont, et al.
Prenatal Diagnosis|March 4, 1998
Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndromeK Devriendt, D Van Schoubroeck, B Eyskens, et al.
Journal of Medical Genetics|May 1, 1997
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeK Devriendt, P Petit, G Matthijs, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhoodS Van Campenhout, K Devriendt, J Breckpot, et al.
Clinical Genetics|June 11, 1999
Partial DiGeorge syndrome in two patients with a 10p rearrangementH Van Esch, P Groenen, S Daw, et al.
AJNR. American Journal of Neuroradiology|December 15, 2012
Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutationsM Elmaleh-Bergès, C Baumann, N Noël-Pétroff, et al.
Pageof 23

Showing results (181-190 of 230) with videos related to

Sort By:
Pageof 23
B-ENT|November 26, 2015
Review: Facial endophenotypes in non-syndromic orofacial cleftingJ Roosenboom, P Claes, K Devriendt, et al.
Annales De Genetique|February 13, 2001
Cryptic translocation t(5;18) in familial mental retardationA Vogels, K Devriendt, J R Vermeesch, et al.
Clinical Genetics|April 1, 1997
Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletionK Devriendt, R Van Hoestenberghe, C Van Hole, et al.
American Journal of Human Genetics|March 1, 1997
Skewed X-chromosome inactivation in female carriers of dyskeratosis congenitaK Devriendt, G Matthijs, E Legius, et al.
Cytogenetic and Genome Research|November 25, 2006
Molecular karyotyping of patients with MCA/MR: the blurred boundary between normal and pathogenic variationT J L de Ravel, I Balikova, B Thienpont, et al.
Prenatal Diagnosis|March 4, 1998
Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndromeK Devriendt, D Van Schoubroeck, B Eyskens, et al.
Journal of Medical Genetics|May 1, 1997
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeK Devriendt, P Petit, G Matthijs, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhoodS Van Campenhout, K Devriendt, J Breckpot, et al.
Clinical Genetics|June 11, 1999
Partial DiGeorge syndrome in two patients with a 10p rearrangementH Van Esch, P Groenen, S Daw, et al.
AJNR. American Journal of Neuroradiology|December 15, 2012
Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutationsM Elmaleh-Bergès, C Baumann, N Noël-Pétroff, et al.
Pageof 23