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J C Albrechts

Showing results (1-10 of 21) with videos related to

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Journal of Medical Genetics|May 23, 1998
A simple and efficient method for microdissection and microFISHJ J Engelen, J C Albrechts, G J Hamers, et al.
American Journal of Medical Genetics|September 24, 1999
Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: value of FISH over high resolution bandingC E de Die-Smulders, J J Engelen, J C Albrechts, et al.
American Journal of Medical Genetics|October 20, 2000
Familial dup(8)(p12p21.1): mild phenotypic effect and review of partial 8p duplicationsU Moog, J J Engelen, J C Albrechts, et al.
American Journal of Medical Genetics|April 6, 2000
Duplication of chromosome region 8p23.1-->p23.3: a benign variant?J J Engelen, U Moog, J L Evers, et al.
American Journal of Medical Genetics|June 22, 2000
Mosaic telomeric (2;14) association in a child with motor delayJ J Engelen, C Marcelis, J Herbergs, et al.
Genomics|July 15, 1997
Assignment of the human gene for smoothelin (SMTN) to chromosome 22q12 by fluorescence in situ hybridization and radiation hybrid mappingJ J Engelen, L E Esterling, J C Albrechts, et al.
Journal of Medical Genetics|July 25, 1998
Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3)A S Plomp, J J Engelen, J C Albrechts, et al.
Cancer Genetics and Cytogenetics|January 20, 2000
Complex chromosome 9, 20, and 22 rearrangements in acute lymphoblastic leukemia with duplication of BCR and ABL sequencesM J Stevens-Kroef, R Dirckx, L E Meers, et al.
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
A patient with a de novo 11q24.2-->qter deletionL Spruijt, J P Fryns, J Hanekom, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Application of micro-FISH to delineate deletionsJ J Engelen, J C Albrechts, W J Loots, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|May 23, 1998
A simple and efficient method for microdissection and microFISHJ J Engelen, J C Albrechts, G J Hamers, et al.
American Journal of Medical Genetics|September 24, 1999
Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: value of FISH over high resolution bandingC E de Die-Smulders, J J Engelen, J C Albrechts, et al.
American Journal of Medical Genetics|October 20, 2000
Familial dup(8)(p12p21.1): mild phenotypic effect and review of partial 8p duplicationsU Moog, J J Engelen, J C Albrechts, et al.
American Journal of Medical Genetics|April 6, 2000
Duplication of chromosome region 8p23.1-->p23.3: a benign variant?J J Engelen, U Moog, J L Evers, et al.
American Journal of Medical Genetics|June 22, 2000
Mosaic telomeric (2;14) association in a child with motor delayJ J Engelen, C Marcelis, J Herbergs, et al.
Genomics|July 15, 1997
Assignment of the human gene for smoothelin (SMTN) to chromosome 22q12 by fluorescence in situ hybridization and radiation hybrid mappingJ J Engelen, L E Esterling, J C Albrechts, et al.
Journal of Medical Genetics|July 25, 1998
Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3)A S Plomp, J J Engelen, J C Albrechts, et al.
Cancer Genetics and Cytogenetics|January 20, 2000
Complex chromosome 9, 20, and 22 rearrangements in acute lymphoblastic leukemia with duplication of BCR and ABL sequencesM J Stevens-Kroef, R Dirckx, L E Meers, et al.
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
A patient with a de novo 11q24.2-->qter deletionL Spruijt, J P Fryns, J Hanekom, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Application of micro-FISH to delineate deletionsJ J Engelen, J C Albrechts, W J Loots, et al.
Pageof 3