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

J Weissenbach

Showing results (171-180 of 363) with videos related to

Pageof 37
Sort By:
Human Molecular Genetics|January 1, 1996
A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23H Chaïb, C Place, N Salem, et al.
Human Molecular Genetics|December 1, 1993
A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellitesJ S Beckmann, J Tomfohrde, R I Barnes, et al.
Clinical Genetics|October 12, 1999
Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?S Fauré, I Bordelais, C Marquette, et al.
Nature|October 24, 1985
Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomesM C Simmler, F Rouyer, G Vergnaud, et al.
Oncogene|May 26, 1999
Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinomaP Pineau, H Nagai, S Prigent, et al.
Cancer Letters|September 25, 1995
Precise mapping of t(12;14) leiomyoma breakpoint on chromosome 14 between D14S298 and D14S540M K Doney, S C Gerken, R Lynch, et al.
Genomics|June 10, 1995
A radiation hybrid map of 95 STSs spanning human chromosome 13qS H Shaw, J E Farr, B A Thiel, et al.
Human Genetics|December 1, 1995
No evidence of genetic heterogeneity in Crouzon craniofacial dysostosisH W Ma, E Lajeunie, M Le Merrer, et al.
American Journal of Human Genetics|January 1, 1995
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2G Stevanin, G Cancel, A Dürr, et al.
Neuromuscular Disorders : NMD|September 1, 1994
Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the geneE Le Guern, N Ravise, M Gugenheim, et al.
Pageof 37

Showing results (171-180 of 363) with videos related to

Sort By:
Pageof 37
Human Molecular Genetics|January 1, 1996
A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23H Chaïb, C Place, N Salem, et al.
Human Molecular Genetics|December 1, 1993
A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellitesJ S Beckmann, J Tomfohrde, R I Barnes, et al.
Clinical Genetics|October 12, 1999
Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?S Fauré, I Bordelais, C Marquette, et al.
Nature|October 24, 1985
Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomesM C Simmler, F Rouyer, G Vergnaud, et al.
Oncogene|May 26, 1999
Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinomaP Pineau, H Nagai, S Prigent, et al.
Cancer Letters|September 25, 1995
Precise mapping of t(12;14) leiomyoma breakpoint on chromosome 14 between D14S298 and D14S540M K Doney, S C Gerken, R Lynch, et al.
Genomics|June 10, 1995
A radiation hybrid map of 95 STSs spanning human chromosome 13qS H Shaw, J E Farr, B A Thiel, et al.
Human Genetics|December 1, 1995
No evidence of genetic heterogeneity in Crouzon craniofacial dysostosisH W Ma, E Lajeunie, M Le Merrer, et al.
American Journal of Human Genetics|January 1, 1995
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2G Stevanin, G Cancel, A Dürr, et al.
Neuromuscular Disorders : NMD|September 1, 1994
Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the geneE Le Guern, N Ravise, M Gugenheim, et al.
Pageof 37