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

B Keats

Showing results (21-30 of 34) with videos related to

Pageof 4
Sort By:
American Journal of Physical Anthropology|May 1, 1977
Genes and people in the Caspian Littoral: a population genetic study in Northern IranR L Kirk, B Keats, N M Blake, et al.
American Journal of Human Genetics|July 21, 2000
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delTA J Griffith, A A Chowdhry, K Kurima, et al.
Nucleic Acids Research|November 10, 2004
Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxiaLaura M Pollard, Rajesh Sharma, Mariluz Gómez, et al.
American Journal of Human Genetics|November 1, 1993
Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19J L Weber, Z Wang, K Hansen, et al.
Journal of the Association for Research in Otolaryngology : JARO|January 28, 2005
A dominantly inherited progressive deafness affecting distal auditory nerve and hair cellsArnold Starr, Brandon Isaacson, Henry J Michalewski, et al.
Neuromuscular Disorders : NMD|July 19, 2003
A novel mitochondrial tRNA(Leu(UUR)) mutation in a patient with features of MERRF and Kearns-Sayre syndromeYutaka Nishigaki, Saba Tadesse, Eduardo Bonilla, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2004
Outline of a medical genetics curriculum for internal medicine residency training programsDouglas L Riegert-Johnson, Bruce R Korf, Raye Lynn Alford, et al.
Child Abuse & Neglect|April 21, 2010
Modification of depression by COMT val158met polymorphism in children exposed to early severe psychosocial deprivationStacy S Drury, Katherine P Theall, Anna T Smyke, et al.
The New England Journal of Medicine|November 20, 1998
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafnessR J Morell, H J Kim, L J Hood, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical GeneticsRaye L Alford, Thomas B Friedman, Bronya J B Keats, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
American Journal of Physical Anthropology|May 1, 1977
Genes and people in the Caspian Littoral: a population genetic study in Northern IranR L Kirk, B Keats, N M Blake, et al.
American Journal of Human Genetics|July 21, 2000
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delTA J Griffith, A A Chowdhry, K Kurima, et al.
Nucleic Acids Research|November 10, 2004
Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxiaLaura M Pollard, Rajesh Sharma, Mariluz Gómez, et al.
American Journal of Human Genetics|November 1, 1993
Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19J L Weber, Z Wang, K Hansen, et al.
Journal of the Association for Research in Otolaryngology : JARO|January 28, 2005
A dominantly inherited progressive deafness affecting distal auditory nerve and hair cellsArnold Starr, Brandon Isaacson, Henry J Michalewski, et al.
Neuromuscular Disorders : NMD|July 19, 2003
A novel mitochondrial tRNA(Leu(UUR)) mutation in a patient with features of MERRF and Kearns-Sayre syndromeYutaka Nishigaki, Saba Tadesse, Eduardo Bonilla, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2004
Outline of a medical genetics curriculum for internal medicine residency training programsDouglas L Riegert-Johnson, Bruce R Korf, Raye Lynn Alford, et al.
Child Abuse & Neglect|April 21, 2010
Modification of depression by COMT val158met polymorphism in children exposed to early severe psychosocial deprivationStacy S Drury, Katherine P Theall, Anna T Smyke, et al.
The New England Journal of Medicine|November 20, 1998
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafnessR J Morell, H J Kim, L J Hood, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical GeneticsRaye L Alford, Thomas B Friedman, Bronya J B Keats, et al.
Pageof 4