R J Morell - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

R J Morell

Showing results (11-20 of 17) with videos related to

Pageof 2

Sort By:

You have reached the last page of results.This site can display upto 17 results.

Science (New York, N.Y.)|June 20, 1998

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, et al.

Science (New York, N.Y.)|June 20, 1998

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgeneF J Probst, R A Fridell, Y Raphael, et al.

Clinical Genetics|September 16, 2016

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.

Cell|February 13, 2001

Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29E R Wilcox, Q L Burton, S Naz, et al.

Journal of Medical Genetics|June 27, 2001

Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafnessT Ben-Yosef, M Wattenhofer, S Riazuddin, et al.

American Journal of Human Genetics|June 21, 2002

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.

American Journal of Human Genetics|November 25, 2000

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.

Pageof 2

Search research articles

Showing results (11-20 of 17) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 17 results.

Science (New York, N.Y.)|June 20, 1998

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, et al.

Science (New York, N.Y.)|June 20, 1998

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgeneF J Probst, R A Fridell, Y Raphael, et al.

Clinical Genetics|September 16, 2016

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.

Cell|February 13, 2001

Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29E R Wilcox, Q L Burton, S Naz, et al.

Journal of Medical Genetics|June 27, 2001

Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafnessT Ben-Yosef, M Wattenhofer, S Riazuddin, et al.

American Journal of Human Genetics|June 21, 2002

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.

American Journal of Human Genetics|November 25, 2000

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.

Pageof 2