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Bronya J B Keats

Showing results (1-10 of 14) with videos related to

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Journal of Communication Disorders|August 6, 2002
Genes and syndromic hearing lossBronya J B Keats
American Journal of Medical Genetics. Part A|September 16, 2004
Genetic heterogeneity in Usher syndromeBronya J B Keats, Sevtap Savas
Journal of the American Academy of Audiology|October 14, 2003
Mouse tales from Kresge: the deafness mouseStacy S Drury, Bronya J B Keats
American Journal of Medical Genetics. Part A|April 12, 2011
HPPD: A newly recognized autosomal dominant disorder involving hypertelorism, preauricular sinus, punctal pits, and deafness mapping to chromosome 14q31Srirangan Sampath, Bronya J B Keats, Yves Lacassie
Journal of Traumatic Stress|December 5, 2009
The role of the dopamine transporter (DAT) in the development of PTSD in preschool childrenStacy S Drury, Katherine P Theall, Bronya J B Keats, et al.
Genomics|February 14, 2004
Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C geneSevtap Savas, Ben Frischhertz, Mark A Batzer, 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.
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.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Journal of Communication Disorders|August 6, 2002
Genes and syndromic hearing lossBronya J B Keats
American Journal of Medical Genetics. Part A|September 16, 2004
Genetic heterogeneity in Usher syndromeBronya J B Keats, Sevtap Savas
Journal of the American Academy of Audiology|October 14, 2003
Mouse tales from Kresge: the deafness mouseStacy S Drury, Bronya J B Keats
American Journal of Medical Genetics. Part A|April 12, 2011
HPPD: A newly recognized autosomal dominant disorder involving hypertelorism, preauricular sinus, punctal pits, and deafness mapping to chromosome 14q31Srirangan Sampath, Bronya J B Keats, Yves Lacassie
Journal of Traumatic Stress|December 5, 2009
The role of the dopamine transporter (DAT) in the development of PTSD in preschool childrenStacy S Drury, Katherine P Theall, Bronya J B Keats, et al.
Genomics|February 14, 2004
Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C geneSevtap Savas, Ben Frischhertz, Mark A Batzer, 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.
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.
Pageof 2