Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M G Mattei

Showing results (71-80 of 427) with videos related to

Pageof 43
Sort By:
Human Genetics|January 19, 1979
Origin of the extra chromosome in trisomy 21J F Mattei, M G Mattei, S Ayme, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1991
Tg (9 HSA-MYC), a homozygous lethal insertion in the mouseS Tutois, J Salaun, M G Mattei, et al.
Human Genetics|January 1, 1981
Partial inversion of the secondary constriction of chromosome 9. Does it exist?M G Mattei, J F Mattei, M Guichaoua, et al.
Human Genetics|January 1, 1981
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: a new technical approachM G Mattei, J F Mattei, I Vidal, et al.
Biochemistry|December 20, 1994
Structure of the mouse dipeptidyl peptidase IV (CD26) geneA M Bernard, M G Mattei, M Pierres, et al.
Genomics|July 9, 1999
PHTF, a novel atypical homeobox gene on chromosome 1p13, is evolutionarily conservedN Raich, M G Mattei, P H Romeo, et al.
Genomics|October 1, 1993
Assignment of the human tear lipocalin gene (LCN1) to 9q34 by in situ hybridizationH Lassagne, C Ressot, M G Mattei, et al.
Human Genetics|March 1, 1990
Assignment by in situ hybridization of the angiotensinogen gene to chromosome band 1q4, the same region as the human renin geneI Gaillard-Sanchez, M G Mattei, E Clauser, et al.
Genomics|October 10, 1995
The human FGF9 gene maps to chromosomal region 13q11-q12M G Mattei, F Penault-Llorca, F Coulier, et al.
Clinical Genetics|September 1, 1983
Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletionJ F Mattei, M G Mattei, P Balestrazzi, et al.
Pageof 43

Showing results (71-80 of 427) with videos related to

Sort By:
Pageof 43
Human Genetics|January 19, 1979
Origin of the extra chromosome in trisomy 21J F Mattei, M G Mattei, S Ayme, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1991
Tg (9 HSA-MYC), a homozygous lethal insertion in the mouseS Tutois, J Salaun, M G Mattei, et al.
Human Genetics|January 1, 1981
Partial inversion of the secondary constriction of chromosome 9. Does it exist?M G Mattei, J F Mattei, M Guichaoua, et al.
Human Genetics|January 1, 1981
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: a new technical approachM G Mattei, J F Mattei, I Vidal, et al.
Biochemistry|December 20, 1994
Structure of the mouse dipeptidyl peptidase IV (CD26) geneA M Bernard, M G Mattei, M Pierres, et al.
Genomics|July 9, 1999
PHTF, a novel atypical homeobox gene on chromosome 1p13, is evolutionarily conservedN Raich, M G Mattei, P H Romeo, et al.
Genomics|October 1, 1993
Assignment of the human tear lipocalin gene (LCN1) to 9q34 by in situ hybridizationH Lassagne, C Ressot, M G Mattei, et al.
Human Genetics|March 1, 1990
Assignment by in situ hybridization of the angiotensinogen gene to chromosome band 1q4, the same region as the human renin geneI Gaillard-Sanchez, M G Mattei, E Clauser, et al.
Genomics|October 10, 1995
The human FGF9 gene maps to chromosomal region 13q11-q12M G Mattei, F Penault-Llorca, F Coulier, et al.
Clinical Genetics|September 1, 1983
Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletionJ F Mattei, M G Mattei, P Balestrazzi, et al.
Pageof 43