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L Messiaen

Showing results (31-40 of 57) with videos related to

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Annales De Genetique|May 26, 1998
Application of fluorescence in situ hybridization to the identification of different marker chromosomesM R Verschraegen-Spae, B Quack, S Rousseaux, et al.
The Journal of Investigative Dermatology|March 25, 2000
arg-cys substitution at codon 1246 of the human myosin Va gene is not associated with Griscelli syndromeJ Lambert, J M Naeyaert, A De Paepe, et al.
In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association|May 1, 1991
Spontaneous acquisition of tumorigenicity and invasiveness by mouse lens explant cells during culture in vitroL Messiaen, S Qian, G De Bruyne, et al.
Clinical Genetics|April 27, 2012
Paraspinal ganglioneuroma in the proband of a large family with mild cutaneous manifestations of NF1, carrying a deep NF1 intronic mutationP Kannu, M Nour, M Irving, et al.
Genetic Testing|September 12, 2001
Carrier screening for cystic fibrosis in a prenatal settingI Delvaux, A van Tongerloo, L Messiaen, et al.
Human Mutation|January 1, 1997
Analysis of 22 cystic fibrosis mutations in 62 patients from the Flanders, Belgium, reveals a high prevalence of Nordic mutation 394delTTL Messiaen, C Van Loon, R Rossau, et al.
Cancer Research|September 1, 1986
Invasiveness and metastatic capability of rat fibroblast-like cells before and after transfection with immortalizing and transforming genesF M Van Roy, L Messiaen, G Liebaut, et al.
European Journal of Medical Genetics|August 12, 2009
Two sporadic spinal neurofibromatosis patients with malignant peripheral nerve sheath tumourC Fauth, H Kehrer-Sawatzki, A Zatkova, et al.
American Journal of Medical Genetics|May 30, 1998
Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactylyW Courtens, W Tjalma, L Messiaen, et al.
Human Mutation|February 22, 2007
Extensive in silico analysis of NF1 splicing defects uncovers determinants for splicing outcome upon 5' splice-site disruptionK Wimmer, X Roca, H Beiglböck, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Annales De Genetique|May 26, 1998
Application of fluorescence in situ hybridization to the identification of different marker chromosomesM R Verschraegen-Spae, B Quack, S Rousseaux, et al.
The Journal of Investigative Dermatology|March 25, 2000
arg-cys substitution at codon 1246 of the human myosin Va gene is not associated with Griscelli syndromeJ Lambert, J M Naeyaert, A De Paepe, et al.
In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association|May 1, 1991
Spontaneous acquisition of tumorigenicity and invasiveness by mouse lens explant cells during culture in vitroL Messiaen, S Qian, G De Bruyne, et al.
Clinical Genetics|April 27, 2012
Paraspinal ganglioneuroma in the proband of a large family with mild cutaneous manifestations of NF1, carrying a deep NF1 intronic mutationP Kannu, M Nour, M Irving, et al.
Genetic Testing|September 12, 2001
Carrier screening for cystic fibrosis in a prenatal settingI Delvaux, A van Tongerloo, L Messiaen, et al.
Human Mutation|January 1, 1997
Analysis of 22 cystic fibrosis mutations in 62 patients from the Flanders, Belgium, reveals a high prevalence of Nordic mutation 394delTTL Messiaen, C Van Loon, R Rossau, et al.
Cancer Research|September 1, 1986
Invasiveness and metastatic capability of rat fibroblast-like cells before and after transfection with immortalizing and transforming genesF M Van Roy, L Messiaen, G Liebaut, et al.
European Journal of Medical Genetics|August 12, 2009
Two sporadic spinal neurofibromatosis patients with malignant peripheral nerve sheath tumourC Fauth, H Kehrer-Sawatzki, A Zatkova, et al.
American Journal of Medical Genetics|May 30, 1998
Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactylyW Courtens, W Tjalma, L Messiaen, et al.
Human Mutation|February 22, 2007
Extensive in silico analysis of NF1 splicing defects uncovers determinants for splicing outcome upon 5' splice-site disruptionK Wimmer, X Roca, H Beiglböck, et al.
Pageof 6