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Author/Creator Turriff, Amy

1. 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
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2. Clinical Features of Optic Disc Drusen in an Ophthalmic Genetics Cohort. (6th October 2020)

Authors:
Serpen, Jasmine Y.; Prasov, Lev; Zein, Wadih M.; Cukras, Catherine A.; Cunningham, Denise; Murphy, Elizabeth C.; Turriff, Amy; Brooks, Brian P.; Huryn, Laryssa A.
Other Names:
Baiocchi Stefano Academic Editor.
Journal:
Journal of ophthalmology
Issue:
Volume 2020(2020)
Page Start:
Record Type:
Journal Article
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6. Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome. Issue 2 (3rd November 2020)

Authors:
Wafa, Talah T.; Faridi, Rabia; King, Kelly A.; Zalewski, Christopher; Yousaf, Rizwan; Schultz, Julie M.; Morell, Robert J.; Muskett, Julie; Turriff, Amy; Tsilou, Ekaterini; Griffith, Andrew J.; Friedman, Thomas B.; Zein, Wadih M.; Brewer, Carmen C.
Journal:
Clinical genetics
Issue:
Volume 99:Issue 2(2021)
Page Start:
226
Record Type:
Journal Article
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