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

H Mehenni

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
Cytogenetic and Genome Research|November 20, 2002
Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2K Buchet-Poyau, H Mehenni, U Radhakrishna, et al.
Gut|January 13, 2006
Cancer risks in LKB1 germline mutation carriersH Mehenni, N Resta, J-G Park, et al.
La Tunisie Medicale|October 1, 1990
[Determination of normal values of the following trace elements: Cu, Mg, Zn in the Tunisian child]S Boukthir, A Hedhili, M F Ben Dridi, et al.
Cytogenetics and Cell Genetics|July 4, 2001
Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndromeA G Marneros, H Mehenni, E Reichenberger, et al.
American Journal of Human Genetics|March 1, 1997
Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysisU Radhakrishna, J L Blouin, H Mehenni, et al.
American Journal of Medical Genetics|July 11, 1997
The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric regionU Radhakrishna, J L Blouin, H Mehenni, et al.
American Journal of Human Genetics|December 5, 1998
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneityH Mehenni, C Gehrig, J Nezu, et al.
American Journal of Human Genetics|December 18, 1997
Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4H Mehenni, J L Blouin, U Radhakrishna, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Cytogenetic and Genome Research|November 20, 2002
Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2K Buchet-Poyau, H Mehenni, U Radhakrishna, et al.
Gut|January 13, 2006
Cancer risks in LKB1 germline mutation carriersH Mehenni, N Resta, J-G Park, et al.
La Tunisie Medicale|October 1, 1990
[Determination of normal values of the following trace elements: Cu, Mg, Zn in the Tunisian child]S Boukthir, A Hedhili, M F Ben Dridi, et al.
Cytogenetics and Cell Genetics|July 4, 2001
Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndromeA G Marneros, H Mehenni, E Reichenberger, et al.
American Journal of Human Genetics|March 1, 1997
Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysisU Radhakrishna, J L Blouin, H Mehenni, et al.
American Journal of Medical Genetics|July 11, 1997
The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric regionU Radhakrishna, J L Blouin, H Mehenni, et al.
American Journal of Human Genetics|December 5, 1998
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneityH Mehenni, C Gehrig, J Nezu, et al.
American Journal of Human Genetics|December 18, 1997
Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4H Mehenni, J L Blouin, U Radhakrishna, et al.
Pageof 1