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Andrew J Griffith

Showing results (71-80 of 109) with videos related to

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Human Genetics|August 11, 2007
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3Quratul Ain, Sabiha Nazli, Saima Riazuddin, et al.
Plos Genetics|October 8, 2011
A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler miceKiyoto Kurima, Ronna Hertzano, Oksana Gavrilova, et al.
Human Genetics|September 5, 2023
CHD7 variants associated with hearing loss and enlargement of the vestibular aqueductIsabelle Roux, Cristina Fenollar-Ferrer, Hyun Jae Lee, et al.
Ophthalmic Genetics|May 7, 2020
Atypical and ultra-rare Usher syndrome: a reviewRosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, et al.
The New England Journal of Medicine|April 15, 2005
Modification of human hearing loss by plasma-membrane calcium pump PMCA2Julie M Schultz, Yandan Yang, Ariel J Caride, et al.
World Journal of Otorhinolaryngology|May 12, 2015
<i>SLC26A4</i> mutation testing for hearing loss associated with enlargement of the vestibular aqueductTaku Ito, Julie Muskett, Parna Chattaraj, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 26, 2011
SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueductTaku Ito, Byung Yoon Choi, Kelly A King, et al.
Nature Genetics|February 19, 2002
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36Sarah Vreugde, Alexandra Erven, Corné J Kros, et al.
Cell Reports|September 1, 2015
TMC1 and TMC2 Localize at the Site of Mechanotransduction in Mammalian Inner Ear Hair Cell StereociliaKiyoto Kurima, Seham Ebrahim, Bifeng Pan, et al.
Journal of the Association for Research in Otolaryngology : JARO|May 20, 2014
Hearing loss is an early consequence of Npc1 gene deletion in the mouse model of Niemann-Pick disease, type CKelly A King, Sandra Gordon-Salant, Karen S Pawlowski, et al.
Pageof 11

Showing results (71-80 of 109) with videos related to

Sort By:
Pageof 11
Human Genetics|August 11, 2007
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3Quratul Ain, Sabiha Nazli, Saima Riazuddin, et al.
Plos Genetics|October 8, 2011
A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler miceKiyoto Kurima, Ronna Hertzano, Oksana Gavrilova, et al.
Human Genetics|September 5, 2023
CHD7 variants associated with hearing loss and enlargement of the vestibular aqueductIsabelle Roux, Cristina Fenollar-Ferrer, Hyun Jae Lee, et al.
Ophthalmic Genetics|May 7, 2020
Atypical and ultra-rare Usher syndrome: a reviewRosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, et al.
The New England Journal of Medicine|April 15, 2005
Modification of human hearing loss by plasma-membrane calcium pump PMCA2Julie M Schultz, Yandan Yang, Ariel J Caride, et al.
World Journal of Otorhinolaryngology|May 12, 2015
<i>SLC26A4</i> mutation testing for hearing loss associated with enlargement of the vestibular aqueductTaku Ito, Julie Muskett, Parna Chattaraj, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 26, 2011
SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueductTaku Ito, Byung Yoon Choi, Kelly A King, et al.
Nature Genetics|February 19, 2002
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36Sarah Vreugde, Alexandra Erven, Corné J Kros, et al.
Cell Reports|September 1, 2015
TMC1 and TMC2 Localize at the Site of Mechanotransduction in Mammalian Inner Ear Hair Cell StereociliaKiyoto Kurima, Seham Ebrahim, Bifeng Pan, et al.
Journal of the Association for Research in Otolaryngology : JARO|May 20, 2014
Hearing loss is an early consequence of Npc1 gene deletion in the mouse model of Niemann-Pick disease, type CKelly A King, Sandra Gordon-Salant, Karen S Pawlowski, et al.
Pageof 11