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C Junien

Showing results (251-260 of 284) with videos related to

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American Journal of Human Genetics|January 1, 1986
Further evidence for the dispersion of the human fibrillar collagen genesC Huerre-Jeanpierre, M G Mattei, D Weil, et al.
Cancer Genetics and Cytogenetics|September 1, 1983
Catalase determination in various etiologic forms of Wilms' tumor and gonadoblastomaC Junien, C Turleau, G M Lenoir, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Fibulin-2: genetic mapping and exclusion as a candidate gene in Marfan syndrome type 2G Collod, M L Chu, T Sasaki, et al.
Human Mutation|January 1, 1992
Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism methodN Loux, B Saint-Jore, G Collod, et al.
Genomics|October 1, 1991
The distal region of 11p13 and associated genetic diseasesM Mannens, J M Hoovers, E M Bleeker-Wagemakers, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1990
Role for the Wilms tumor gene in genital development?V van Heyningen, W A Bickmore, A Seawright, et al.
Hormone Research|July 15, 2000
Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinismJ C Fournet, C Mayaud, P de Lonlay, et al.
Cell|October 18, 1991
Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndromeJ Pelletier, W Bruening, C E Kashtan, et al.
Genomics|November 1, 1989
CpG islands surround a DNA segment located between translocation breakpoints associated with genitourinary dysplasia and aniridiaW A Bickmore, D J Porteous, S Christie, et al.
American Journal of Human Genetics|June 13, 1998
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation databaseC Jeanpierre, E Denamur, I Henry, et al.
Pageof 29

Showing results (251-260 of 284) with videos related to

Sort By:
Pageof 29
American Journal of Human Genetics|January 1, 1986
Further evidence for the dispersion of the human fibrillar collagen genesC Huerre-Jeanpierre, M G Mattei, D Weil, et al.
Cancer Genetics and Cytogenetics|September 1, 1983
Catalase determination in various etiologic forms of Wilms' tumor and gonadoblastomaC Junien, C Turleau, G M Lenoir, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Fibulin-2: genetic mapping and exclusion as a candidate gene in Marfan syndrome type 2G Collod, M L Chu, T Sasaki, et al.
Human Mutation|January 1, 1992
Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism methodN Loux, B Saint-Jore, G Collod, et al.
Genomics|October 1, 1991
The distal region of 11p13 and associated genetic diseasesM Mannens, J M Hoovers, E M Bleeker-Wagemakers, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1990
Role for the Wilms tumor gene in genital development?V van Heyningen, W A Bickmore, A Seawright, et al.
Hormone Research|July 15, 2000
Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinismJ C Fournet, C Mayaud, P de Lonlay, et al.
Cell|October 18, 1991
Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndromeJ Pelletier, W Bruening, C E Kashtan, et al.
Genomics|November 1, 1989
CpG islands surround a DNA segment located between translocation breakpoints associated with genitourinary dysplasia and aniridiaW A Bickmore, D J Porteous, S Christie, et al.
American Journal of Human Genetics|June 13, 1998
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation databaseC Jeanpierre, E Denamur, I Henry, et al.
Pageof 29