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

G M Duyk

Showing results (11-20 of 27) with videos related to

Pageof 3
Sort By:
Nature Genetics|April 1, 1994
Integrated human genome-wide maps constructed using the CEPH reference panelK H Buetow, J L Weber, S Ludwigsen, et al.
Human Molecular Genetics|August 1, 1994
Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mappingV C Sheffield, R Carmi, A Kwitek-Black, et al.
Nature Genetics|December 1, 1993
Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneityA E Kwitek-Black, R Carmi, G M Duyk, et al.
Science (New York, N.Y.)|September 30, 1994
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)J C Murray, K H Buetow, J L Weber, et al.
Genomics|June 10, 1995
cDNA cloning, tissue distribution, and chromosomal localization of Ocp2, a gene encoding a putative transcription-associated factor predominantly expressed in the auditory organsH Chen, I Thalmann, J C Adams, et al.
Science (New York, N.Y.)|September 30, 1994
Human genetic map. Genome maps V. Wall chartK H Buetow, S Ludwigsen, T Scherpbier-Heddema, et al.
Human Molecular Genetics|October 1, 1995
Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markersJ M Gastier, J C Pulido, S Sunden, et al.
Genomics|February 15, 1997
The physical and genetic map surrounding the Lyst gene on mouse chromosome 13D J Misumi, D L Nagle, S H McGrail, et al.
Neuron|January 1, 1996
Periventricular heterotopia: an X-linked dominant epilepsy locus causing aberrant cerebral cortical developmentY Z Ekşioğlu, I E Scheffer, P Cardenas, et al.
Genomics|February 15, 1996
Development of a screening set for new (CAG/CTG)n dynamic mutationsJ M Gastier, T Brody, J C Pulido, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Nature Genetics|April 1, 1994
Integrated human genome-wide maps constructed using the CEPH reference panelK H Buetow, J L Weber, S Ludwigsen, et al.
Human Molecular Genetics|August 1, 1994
Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mappingV C Sheffield, R Carmi, A Kwitek-Black, et al.
Nature Genetics|December 1, 1993
Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneityA E Kwitek-Black, R Carmi, G M Duyk, et al.
Science (New York, N.Y.)|September 30, 1994
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)J C Murray, K H Buetow, J L Weber, et al.
Genomics|June 10, 1995
cDNA cloning, tissue distribution, and chromosomal localization of Ocp2, a gene encoding a putative transcription-associated factor predominantly expressed in the auditory organsH Chen, I Thalmann, J C Adams, et al.
Science (New York, N.Y.)|September 30, 1994
Human genetic map. Genome maps V. Wall chartK H Buetow, S Ludwigsen, T Scherpbier-Heddema, et al.
Human Molecular Genetics|October 1, 1995
Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markersJ M Gastier, J C Pulido, S Sunden, et al.
Genomics|February 15, 1997
The physical and genetic map surrounding the Lyst gene on mouse chromosome 13D J Misumi, D L Nagle, S H McGrail, et al.
Neuron|January 1, 1996
Periventricular heterotopia: an X-linked dominant epilepsy locus causing aberrant cerebral cortical developmentY Z Ekşioğlu, I E Scheffer, P Cardenas, et al.
Genomics|February 15, 1996
Development of a screening set for new (CAG/CTG)n dynamic mutationsJ M Gastier, T Brody, J C Pulido, et al.
Pageof 3