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Author/Creator Griffith, Andrew J

1. A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct. Issue 10 (5th August 2017)

Authors:
Chattaraj, Parna; Munjal, Tina; Honda, Keiji; Rendtorff, Nanna D; Ratay, Jessica S; Muskett, Julie A; Risso, Davide S; Roux, Isabelle; Gertz, E Michael; Schäffer, Alejandro A; Friedman, Thomas B; Morell, Robert J; Tranebjærg, Lisbeth; Griffith, Andrew J
Journal:
Journal of medical genetics
Issue:
Volume 54:Issue 10(2017)
Page Start:
665
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes. Issue 11 (22nd September 2011)

Authors:
Schultz, Julie M; Bhatti, Rashid; Madeo, Anne C; Turriff, Amy; Muskett, Julie A; Zalewski, Christopher K; King, Kelly A; Ahmed, Zubair M; Riazuddin, Saima; Ahmad, Nazir; Hussain, Zawar; Qasim, Muhammad; Kahn, Shaheen N; Meltzer, Meira R; Liu, Xue Z; Munisamy, Murali; Ghosh, Manju; Rehm, Heidi L; ...
Journal:
Journal of medical genetics
Issue:
Volume 48:Issue 11(2011)
Page Start:
767
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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