Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

K Devriendt

Showing results (131-140 of 230) with videos related to

Pageof 23
Sort By:
Genetic Counseling (Geneva, Switzerland)|June 21, 2008
Cognitive correlates of mathematical disabilities in children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.
Human Genetics|November 1, 1989
Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome. Construction of a mouse-human hybrid cell line containing an i(12p) as the sole human chromosomeJ Zhang, P Marynen, K Devriendt, et al.
American Journal of Medical Genetics|February 7, 1998
Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50)S Claes, A Vogels, M Holvoet, et al.
Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopiaC P Chen, K Devriendt, C C Lee, et al.
Prenatal Diagnosis|May 23, 2000
Prenatal diagnosis of inherited satellited non-acrocentric chromosomesC P Chen, K Devriendt, S R Chern, et al.
American Journal of Medical Genetics|July 9, 1999
Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1S Claes, P Volcke, K Devriendt, et al.
Bulletin De La Societe Belge D'Ophtalmologie|December 24, 1998
Genetics in ophthalmologyA Bergen, K Devriendt, L Messiaen, et al.
European Journal of Pediatrics|October 1, 1994
Asplenia syndrome and isolated total anomalous pulmonary venous connection in siblingsK Devriendt, A Casaer, A Van Cauter, et al.
Clinical Genetics|March 21, 2002
Autosomal dominant isolated velopharyngeal insufficiencyG Vantrappen, N Rommel, W Wellens, et al.
American Journal of Human Genetics|June 12, 1999
Haploinsufficiency of the HOXA gene cluster, in a patient with hand-foot-genital syndrome, velopharyngeal insufficiency, and persistent patent Ductus botalliK Devriendt, J Jaeken, G Matthijs, et al.
Pageof 23

Showing results (131-140 of 230) with videos related to

Sort By:
Pageof 23
Genetic Counseling (Geneva, Switzerland)|June 21, 2008
Cognitive correlates of mathematical disabilities in children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.
Human Genetics|November 1, 1989
Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome. Construction of a mouse-human hybrid cell line containing an i(12p) as the sole human chromosomeJ Zhang, P Marynen, K Devriendt, et al.
American Journal of Medical Genetics|February 7, 1998
Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50)S Claes, A Vogels, M Holvoet, et al.
Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopiaC P Chen, K Devriendt, C C Lee, et al.
Prenatal Diagnosis|May 23, 2000
Prenatal diagnosis of inherited satellited non-acrocentric chromosomesC P Chen, K Devriendt, S R Chern, et al.
American Journal of Medical Genetics|July 9, 1999
Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1S Claes, P Volcke, K Devriendt, et al.
Bulletin De La Societe Belge D'Ophtalmologie|December 24, 1998
Genetics in ophthalmologyA Bergen, K Devriendt, L Messiaen, et al.
European Journal of Pediatrics|October 1, 1994
Asplenia syndrome and isolated total anomalous pulmonary venous connection in siblingsK Devriendt, A Casaer, A Van Cauter, et al.
Clinical Genetics|March 21, 2002
Autosomal dominant isolated velopharyngeal insufficiencyG Vantrappen, N Rommel, W Wellens, et al.
American Journal of Human Genetics|June 12, 1999
Haploinsufficiency of the HOXA gene cluster, in a patient with hand-foot-genital syndrome, velopharyngeal insufficiency, and persistent patent Ductus botalliK Devriendt, J Jaeken, G Matthijs, et al.
Pageof 23