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L Messiaen

Showing results (1-10 of 57) with videos related to

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Haemostasis|August 5, 1998
Identification of two different mutations causing protein S deficiency in two unrelated Belgian families using a nonisotopic scanning and sequencing methodL Messiaen, T Callens, G Baele
Clinical Genetics|October 26, 2016
Connections between constitutional mismatch repair deficiency syndrome and neurofibromatosis type 1K Wimmer, T Rosenbaum, L Messiaen
Cytotechnology|February 24, 2012
Anin vitro model for chick embryonic notochordsE Ghanem, L Messiaen, L De Ridder
Nucleic Acids Research|July 4, 2001
Quantification of splice variants using real-time PCRI I Vandenbroucke, J Vandesompele, A D Paepe, et al.
DNA and Cell Biology|March 10, 2001
Cloning and characterization of human WDR10, a novel gene located at 3q21 encoding a WD-repeat protein that is highly expressed in pituitary and testisC Gross, E De Baere, A Lo, et al.
British Journal of Cancer|March 18, 2004
BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer familiesK Claes, B Poppe, I Coene, et al.
Genetic Counseling (Geneva, Switzerland)|October 23, 2010
Coexistence of neurofibromatosis type 1 and mosaic trisomy 8 in the same patientS Y Basaran, V Sensoy, K Kiroglu, et al.
Human Genetics|January 7, 1998
Characterisation of two different nonsense mutations, C6792A and C6792G, causing skipping of exon 37 in the NF1 geneL Messiaen, T Callens, A De Paepe, et al.
Casopis Lekaru Ceskych|February 24, 2001
A high occurrence of BRCA1 and BRCA2 mutations among Czech hereditary breast and breast-ovarian cancer familiesE Machácková, L Foretová, M Navrátilová, et al.
Acta Gastro-Enterologica Belgica|February 24, 2001
Prevalence of the Cys282Tyr and His63Asp mutation in Flemish patients with hereditary hemochromatosisH Van Vlierberghe, L Messiaen, M Hautekeete, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Haemostasis|August 5, 1998
Identification of two different mutations causing protein S deficiency in two unrelated Belgian families using a nonisotopic scanning and sequencing methodL Messiaen, T Callens, G Baele
Clinical Genetics|October 26, 2016
Connections between constitutional mismatch repair deficiency syndrome and neurofibromatosis type 1K Wimmer, T Rosenbaum, L Messiaen
Cytotechnology|February 24, 2012
Anin vitro model for chick embryonic notochordsE Ghanem, L Messiaen, L De Ridder
Nucleic Acids Research|July 4, 2001
Quantification of splice variants using real-time PCRI I Vandenbroucke, J Vandesompele, A D Paepe, et al.
DNA and Cell Biology|March 10, 2001
Cloning and characterization of human WDR10, a novel gene located at 3q21 encoding a WD-repeat protein that is highly expressed in pituitary and testisC Gross, E De Baere, A Lo, et al.
British Journal of Cancer|March 18, 2004
BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer familiesK Claes, B Poppe, I Coene, et al.
Genetic Counseling (Geneva, Switzerland)|October 23, 2010
Coexistence of neurofibromatosis type 1 and mosaic trisomy 8 in the same patientS Y Basaran, V Sensoy, K Kiroglu, et al.
Human Genetics|January 7, 1998
Characterisation of two different nonsense mutations, C6792A and C6792G, causing skipping of exon 37 in the NF1 geneL Messiaen, T Callens, A De Paepe, et al.
Casopis Lekaru Ceskych|February 24, 2001
A high occurrence of BRCA1 and BRCA2 mutations among Czech hereditary breast and breast-ovarian cancer familiesE Machácková, L Foretová, M Navrátilová, et al.
Acta Gastro-Enterologica Belgica|February 24, 2001
Prevalence of the Cys282Tyr and His63Asp mutation in Flemish patients with hereditary hemochromatosisH Van Vlierberghe, L Messiaen, M Hautekeete, et al.
Pageof 6