Search Results

Molecular genetics of Bardet-Biedl syndrome (BBS) in the Newfoundland population

by Young, Terry-Lynn
Published 2000

Effects of several insect growth regulators on the cabbage maggot, Delia radicum Linnaeus (Diptera: Anthomyiidae)

by Young, Terry-Lynn, 1961-
Published 1988

Molecular genetics of Bardet-Biedl syndrome (BBS) in the Newfoundland population

by Young, Terry-Lynn, 1961-
Published 2000

Translation of research discoveries to clinical care in arrhythmogenic right ventricular cardiomyopathy in Newfoundland and Labrador: Lessons for health policy in genetic disease

by Hodgkinson, Kathy, Dicks, Elizabeth, Connors, Sean, Young, Terry-Lynn, Parfrey, Patrick, Pullman, Daryl
Published in Genetics in Medicine (2009)

Translation of research discoveries to clinical care in arrhythmogenic right ventricular cardiomyopathy in Newfoundland and Labrador: Lessons for health policy in genetic disease

by Hodgkinson, Kathy, Dicks, Elizabeth, Connors, Sean, Young, Terry-Lynn, Parfrey, Patrick, Pullman, Daryl
Published in Genetics in Medicine (2009)

SCOPE AND NATURE OF YOUNG SUDDEN CARDIAC DEATH IN NEWFOUNDLAND & LABRADOR

by Hamilton, Gina, Avis, Simon, Curtis, Fiona, Young, Terry-Lynn, Connors, Sean, Hodgkinson, Kathleen
Published in Journal of Epidemiology and Community Health (2013)

A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly

by Doucette, Lance, Green, Jane, Fernandez, Bridget, Johnson, Gordon J, Parfrey, Patrick, Young, Terry-Lynn
Published in European Journal of Human Genetics (2011)

A Founder Effect in the Newfoundland Population Reduces the Bardet-Biedl Syndrome I (BBS1) Interval to 1 cM

by Young, Terry-Lynn, Woods, Michael O., Parfrey, Patrick S., Green, Jane S., Hefferton, Donna, Davidson, William S.
Published in The American Journal of Human Genetics (1999)

A Founder Effect in the Newfoundland Population Reduces the Bardet-Biedl Syndrome I (BBS1) Interval to 1 cM

by Young, Terry-Lynn, Woods, Michael O., Parfrey, Patrick S., Green, Jane S., Hefferton, Donna, Davidson, William S.
Published 1999

Molecular Genetics of Achromatopsia in Newfoundland Reveal Genetic Heterogeneity, Founder Effects and the First Cases of Jalili Syndrome in North America

by Doucette, Lance, Green, Jane, Black, Coleman, Schwartzentruber, Jeremy, Johnson, Gordon J., Galutira, Dante, Young, Terry-Lynn
Published in Ophthalmic Genetics (2013)

High incidence of pediatric idiopathic epilepsy is associated with familial and autosomal dominant disease in Eastern Newfoundland

by Mahoney, Krista, Buckley, David, Alam, Muhammed, Penney, Sharon, Young, Terry-Lynn, Parfrey, Patrick, Moore, Susan J.
Published in Epilepsy Research (2012)

Psychological Distress and Quality of Life in Participants Undergoing Genetic Testing for Arrhythmogenic Right Ventricular Cardiomyopathy Caused by TMEM43 p.S358L: Is It Time to Of...

by Brothers, Cassidy, Etchegary, Holly, Curtis, Fiona, Simmonds, Charlene, Houston, Jim, Young, Terry-Lynn, Pullman, Daryl, Mariathas, Hensley H., Connors, Sean, Hodgkinson, Kathleen
Published in Public Health Genomics (2021)

A preliminary analysis of the DNA and diet of the extinct Beothuk: a systematic approach to ancient human DNA.

by Kuch, Melanie, Gröcke, Darren R, Knyf, Martin C, Gilbert, M Thomas P, Younghusband, Ban, Young, Terry, Marshall, Ingeborg, Willerslev, Eske, Stoneking, Mark, Poinar, Hendrik
Published in American Journal of Physical Anthropology (2007)

A preliminary analysis of the DNA and diet of the extinct Beothuk: A systematic approach to ancient human DNA

by Kuch, Melanie, Gröcke, Darren R., Knyf, Martin C., Gilbert, M. Thomas P., Younghusband, Ban, Young, Terry, Marshall, Ingeborg, Willerslev, Eske, Stoneking, Mark, Poinar, Hendrik
Published in American Journal of Physical Anthropology (2007)

Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

by Young, Terry-Lynn, Ives, Elizabeth, Lynch, Eric, Person, Richard, Snook, Stephanie, MacLaren, Linda, Cator, Tracey, Griffin, Anne, Fernandez, Bridget, Lee, Ming K., King, Mary-Claire
Published in Human Molecular Genetics (2001)

“Something is just not right with my hearing”: early experiences of adults living with hearing loss

by Pike, April, Moodie, Sheila, Parsons, Karen, Griffin, Anne, Smith-Young, Joanne, Young, Terry-Lynn, Mills, Leon, Barrett, Myrtle, Rowe, Leanna, Parsons, Marie, Kielley, Henry, Fleming, Michael
Published 2021

“Something is just not right with my hearing”: early experiences of adults living with hearing loss

by Pike, April, Moodie, Sheila, Parsons, Karen, Griffin, Anne, Smith-Young, Joanne, Young, Terry-Lynn, Mills, Leon, Barrett, Myrtle, Rowe, Leanna, Parsons, Marie, Kielley, Henry, Fleming, Michael
Published 2021

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene

by Pater, Justin A., Penney, Cindy, O’Rielly, Darren D., Griffin, Anne, Kamal, Lara, Brownstein, Zippora, Vona, Barbara, Vinkler, Chana, Shohat, Mordechai, Barel, Ortal, Young, Terry-Lynn
Published in Human Genetics (2022)

The genetic architecture of Stargardt macular dystrophy (STGD1): a longitudinal 40-year study in a genetic isolate

by Green, Jane S., O’Rielly, Darren D., Pater, Justin A., Houston, Jim, Rajabi, Hoda, Galutira, Dante, Benteau, Tammy, Sheaves, Amy, Abdelfatah, Nelly, Bautista, Donna, Whelan, Jim, Young, Terry-Lynn
Published in European Journal of Human Genetics (2020)

Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada

by Haywood, Annika, Merner, Nancy D., Hodgkinson, Kathy A., Houston, Jim, Syrris, Petros, Booth, Valerie, Connors, Sean, Pantazis, Antonios, Quarta, Giovanni, Elliott, Perry, McKenna, William, Young, Terry Lynn
Published in European Heart Journal (2012)