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R Verschraegen

Showing results (31-40 of 36) with videos related to

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American Journal of Medical Genetics|June 14, 1996
Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomaliesA Van den Enden, M R Verschraegen-Spae, N Van Roy, et al.
Human Reproduction (Oxford, England)|April 29, 1998
Fluorescent in-situ hybridization on human embryos showing cleavage arrest after freezing and thawingH Laverge, J Van der Elst, P De Sutter, et al.
Clinical Genetics|April 1, 1992
Detection of subtle reciprocal translocations by fluorescence in situ hybridizationF Speleman, N Van Roy, J Wiegant, et al.
American Journal of Medical Genetics|August 22, 2000
Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35-->qter: molecular cytogenetic analysis and clinical phenotype in two generationsF Speleman, B Callens, K Logghe, et al.
American Journal of Medical Genetics|December 1, 1991
Pallister-Killian syndrome: characterization of the isochromosome 12p by fluorescent in situ hybridizationF Speleman, J G Leroy, N Van Roy, et al.
American Journal of Medical Genetics|July 1, 1994
Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studiesW Courtens, M B Petersen, J C Noël, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
American Journal of Medical Genetics|June 14, 1996
Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomaliesA Van den Enden, M R Verschraegen-Spae, N Van Roy, et al.
Human Reproduction (Oxford, England)|April 29, 1998
Fluorescent in-situ hybridization on human embryos showing cleavage arrest after freezing and thawingH Laverge, J Van der Elst, P De Sutter, et al.
Clinical Genetics|April 1, 1992
Detection of subtle reciprocal translocations by fluorescence in situ hybridizationF Speleman, N Van Roy, J Wiegant, et al.
American Journal of Medical Genetics|August 22, 2000
Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35-->qter: molecular cytogenetic analysis and clinical phenotype in two generationsF Speleman, B Callens, K Logghe, et al.
American Journal of Medical Genetics|December 1, 1991
Pallister-Killian syndrome: characterization of the isochromosome 12p by fluorescent in situ hybridizationF Speleman, J G Leroy, N Van Roy, et al.
American Journal of Medical Genetics|July 1, 1994
Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studiesW Courtens, M B Petersen, J C Noël, et al.
Pageof 4