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J J Engelen

Showing results (41-50 of 49) with videos related to

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American Journal of Medical Genetics|March 3, 1998
Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridizationJ J Engelen, W J Loots, J C Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Phenotypic variability of the cat eye syndrome. Case report and review of the literatureP R Rosias, J M Sijstermans, P M Theunissen, et al.
Clinical Genetics|April 1, 1994
Partial trisomy and monosomy 8p due to inversion duplicationJ J Engelen, C E de Die-Smulders, J P Fryns, et al.
Genetic Counseling (Geneva, Switzerland)|January 5, 2001
14q terminal deletion: prenatal diagnosis in a child with severe congenital anomaliesD J Mertens, C E De Die-Smulders, P H Kampschöer, et al.
Clinical Genetics|September 1, 1996
Deletion of the long arm of chromosome 6: two new patients and literature reviewL J Evers, C T Schrander-Stumpel, J J Engelen, et al.
Human Molecular Genetics|April 1, 1994
A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndromeH Meijer, E de Graaff, D M Merckx, et al.
Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Strong variable clinical presentation in 3 patients with 7q terminal deletionS G Frints, C T Schrander-Stumpel, E F Schoenmakers, et al.
American Journal of Medical Genetics|November 20, 1995
Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literatureC E de Die-Smulders, J J Engelen, C T Schrander-Stumpel, et al.
American Journal of Medical Genetics|May 1, 1994
Mosaic tetrasomy 8p in two patients: clinical data and review of the literatureC T Schrander-Stumpel, L C Govaerts, J J Engelen, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
American Journal of Medical Genetics|March 3, 1998
Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridizationJ J Engelen, W J Loots, J C Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Phenotypic variability of the cat eye syndrome. Case report and review of the literatureP R Rosias, J M Sijstermans, P M Theunissen, et al.
Clinical Genetics|April 1, 1994
Partial trisomy and monosomy 8p due to inversion duplicationJ J Engelen, C E de Die-Smulders, J P Fryns, et al.
Genetic Counseling (Geneva, Switzerland)|January 5, 2001
14q terminal deletion: prenatal diagnosis in a child with severe congenital anomaliesD J Mertens, C E De Die-Smulders, P H Kampschöer, et al.
Clinical Genetics|September 1, 1996
Deletion of the long arm of chromosome 6: two new patients and literature reviewL J Evers, C T Schrander-Stumpel, J J Engelen, et al.
Human Molecular Genetics|April 1, 1994
A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndromeH Meijer, E de Graaff, D M Merckx, et al.
Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Strong variable clinical presentation in 3 patients with 7q terminal deletionS G Frints, C T Schrander-Stumpel, E F Schoenmakers, et al.
American Journal of Medical Genetics|November 20, 1995
Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literatureC E de Die-Smulders, J J Engelen, C T Schrander-Stumpel, et al.
American Journal of Medical Genetics|May 1, 1994
Mosaic tetrasomy 8p in two patients: clinical data and review of the literatureC T Schrander-Stumpel, L C Govaerts, J J Engelen, et al.
Pageof 5