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L Messiaen

Showing results (21-30 of 57) with videos related to

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British Journal of Cancer|November 28, 2002
Chromosomal radiosensitivity in breast cancer patients with a known or putative genetic predispositionA Baeyens, H Thierens, K Claes, et al.
The Journal of Rheumatology|September 16, 2000
Occurrence of scleroderma in monozygotic twinsF De Keyser, I Peene, R Joos, et al.
Genomics|April 7, 1999
Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpointE De Baere, N Van Roy, F Speleman, et al.
Cytogenetics and Cell Genetics|March 11, 1999
Assignment of the cellular retinol-binding protein 2 gene (RBP2) to human chromosome band 3q23 by in situ hybridizationE De Baere, F Speleman, N Van Roy, et al.
Clinical Genetics|March 16, 2017
Constitutional LZTR1 mutation presenting with a unilateral vestibular schwannoma in a teenagerK W Gripp, L Baker, V Kandula, et al.
Journal of Medical Genetics|August 6, 2002
FOXL2 mutation screening in a large panel of POF patients and XX malesE De Baere, B Lemercier, S Christin-Maitre, et al.
Bulletin De La Societe Belge D'Ophtalmologie|December 24, 1998
Genetics in ophthalmologyA Bergen, K Devriendt, L Messiaen, et al.
Disease Markers|December 14, 1999
Genetic counselling and testing for hereditary breast and ovarian cancer: the gent(le) approachM De Vos, B Poppe, I Delvaux, et al.
The British Journal of Dermatology|July 17, 2016
Mosaicism for a SPRED1 deletion revealed in a patient with clinically suspected mosaic neurofibromatosisR K Jobling, I Lara-Corrales, M-C Hsiao, et al.
Pathology, Research and Practice|February 1, 1987
Pathology of tumours produced in syngeneic Fischer rats by fibroblast-like cells before and after transfection with oncogenesJ Gao, F Van Roy, L Messiaen, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
British Journal of Cancer|November 28, 2002
Chromosomal radiosensitivity in breast cancer patients with a known or putative genetic predispositionA Baeyens, H Thierens, K Claes, et al.
The Journal of Rheumatology|September 16, 2000
Occurrence of scleroderma in monozygotic twinsF De Keyser, I Peene, R Joos, et al.
Genomics|April 7, 1999
Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpointE De Baere, N Van Roy, F Speleman, et al.
Cytogenetics and Cell Genetics|March 11, 1999
Assignment of the cellular retinol-binding protein 2 gene (RBP2) to human chromosome band 3q23 by in situ hybridizationE De Baere, F Speleman, N Van Roy, et al.
Clinical Genetics|March 16, 2017
Constitutional LZTR1 mutation presenting with a unilateral vestibular schwannoma in a teenagerK W Gripp, L Baker, V Kandula, et al.
Journal of Medical Genetics|August 6, 2002
FOXL2 mutation screening in a large panel of POF patients and XX malesE De Baere, B Lemercier, S Christin-Maitre, et al.
Bulletin De La Societe Belge D'Ophtalmologie|December 24, 1998
Genetics in ophthalmologyA Bergen, K Devriendt, L Messiaen, et al.
Disease Markers|December 14, 1999
Genetic counselling and testing for hereditary breast and ovarian cancer: the gent(le) approachM De Vos, B Poppe, I Delvaux, et al.
The British Journal of Dermatology|July 17, 2016
Mosaicism for a SPRED1 deletion revealed in a patient with clinically suspected mosaic neurofibromatosisR K Jobling, I Lara-Corrales, M-C Hsiao, et al.
Pathology, Research and Practice|February 1, 1987
Pathology of tumours produced in syngeneic Fischer rats by fibroblast-like cells before and after transfection with oncogenesJ Gao, F Van Roy, L Messiaen, et al.
Pageof 6