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Young, Terry-Lynn
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Young, Terry-Lynn
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Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is cause...
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The genetic architecture of Stargardt macular dystrophy (STGD1): a longitudinal...
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Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of mu...
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A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variabl...
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Characterization of a new full length TMPRSS3 isoform and identification of muta...
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A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing...
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A Founder Effect in the Newfoundland Population Reduces the Bardet-Biedl Syndrom...
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Author
Young, Terry-Lynn
Abdelfatah, Nelly
3
Doucette, Lance
3
Benteau, Tammy
2
Fernandez, Bridget
2
Galutira, Dante
2
Green, Jane S.
2
Griffin, Anne
2
Houston, Jim
2
Ives, Elizabeth
2
MacLaren, Linda
2
O’Rielly, Darren D.
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Pater, Justin A.
2
Wilcox, Edward R
2
Ahmad, Zahoor
1
Ahmed, Zubair M
1
Bautista, Donna
1
Cater, Tracey
1
Cindy Li, Xiaoyan
1
Cooke, Sandra
1
Davidson, William S.
1
Dhillon, Kiran
1
Friedman, Thomas B
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Green, Jane
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Green, Jane S
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Hefferton, Donna
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Hodgkinson, Kathy A
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Johnson, Gordon J
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Kielley, Bernadine
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King, Justin J
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PubMed Central (PMC)
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7
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Newfoundland
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