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J C Albrechts

Showing results (11-20 of 21) with videos related to

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Annales De Genetique|August 6, 1999
Characterization of a partial trisomy 16q with FISH. Report of a patient and review of the literatureJ J Engelen, C E De Die-Smulders, P T Vos, et al.
Genomics|November 10, 1998
Assignment of the human gene for the sarcomeric M-band protein myomesin (MYOM1) to 18p11.31-p11.32E J Speel, P F van der Ven, J C Albrechts, et al.
Journal of Medical Genetics|October 1, 1995
Familial partial trisomy 8p without dysmorphic features and only mild mental retardationJ J Engelen, C E de Die-Smulders, J M Sijstermans, et al.
Genomics|February 6, 1999
Assignment of the human gene for endosarcomeric cytoskeletal M-protein (MYOM2) to 8p23.3P F van der Ven, E J Speel, J C Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)|April 11, 2000
Prenatally detected marker chromosome identified as an i(22)(p10) using (micro)FISHJ J Engelen, J H Tuerlings, J C Albrechts, et al.
Journal of Medical Genetics|July 1, 1996
Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISHJ J Engelen, W J Loots, J C Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fishJ J Engelen, W J Loots, J C Albrechts, et al.
Clinical Genetics|December 1, 1994
Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplicationU Moog, J J Engelen, C E de Die-Smulders, et al.
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.
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.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Annales De Genetique|August 6, 1999
Characterization of a partial trisomy 16q with FISH. Report of a patient and review of the literatureJ J Engelen, C E De Die-Smulders, P T Vos, et al.
Genomics|November 10, 1998
Assignment of the human gene for the sarcomeric M-band protein myomesin (MYOM1) to 18p11.31-p11.32E J Speel, P F van der Ven, J C Albrechts, et al.
Journal of Medical Genetics|October 1, 1995
Familial partial trisomy 8p without dysmorphic features and only mild mental retardationJ J Engelen, C E de Die-Smulders, J M Sijstermans, et al.
Genomics|February 6, 1999
Assignment of the human gene for endosarcomeric cytoskeletal M-protein (MYOM2) to 8p23.3P F van der Ven, E J Speel, J C Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)|April 11, 2000
Prenatally detected marker chromosome identified as an i(22)(p10) using (micro)FISHJ J Engelen, J H Tuerlings, J C Albrechts, et al.
Journal of Medical Genetics|July 1, 1996
Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISHJ J Engelen, W J Loots, J C Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fishJ J Engelen, W J Loots, J C Albrechts, et al.
Clinical Genetics|December 1, 1994
Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplicationU Moog, J J Engelen, C E de Die-Smulders, et al.
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.
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.
Pageof 3