A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort

Bibliographic Details
Published in:Journal of Medical Genetics
Main Authors: Elliott, Alison M, Simard, Louise R, Coghlan, Gail, Chudley, Albert E, Chodirker, Bernard N, Greenberg, Cheryl R, Burch, Tanya, Ly, Valentina, Hatch, Grant M, Zelinski, Teresa
Format: Article in Journal/Newspaper
Language:English
Published: BMJ 2013
Subjects:
Online Access:http://dx.doi.org/10.1136/jmedgenet-2013-101715
https://syndication.highwire.org/content/doi/10.1136/jmedgenet-2013-101715
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spelling crjcrbmj:10.1136/jmedgenet-2013-101715 2024-09-15T18:06:24+00:00 A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort Elliott, Alison M Simard, Louise R Coghlan, Gail Chudley, Albert E Chodirker, Bernard N Greenberg, Cheryl R Burch, Tanya Ly, Valentina Hatch, Grant M Zelinski, Teresa 2013 http://dx.doi.org/10.1136/jmedgenet-2013-101715 https://syndication.highwire.org/content/doi/10.1136/jmedgenet-2013-101715 en eng BMJ Journal of Medical Genetics volume 50, issue 12, page 819-822 ISSN 0022-2593 1468-6244 journal-article 2013 crjcrbmj https://doi.org/10.1136/jmedgenet-2013-101715 2024-08-08T04:21:45Z Article in Journal/Newspaper First Nations The BMJ Journal of Medical Genetics 50 12 819 822
institution Open Polar
collection The BMJ
op_collection_id crjcrbmj
language English
format Article in Journal/Newspaper
author Elliott, Alison M
Simard, Louise R
Coghlan, Gail
Chudley, Albert E
Chodirker, Bernard N
Greenberg, Cheryl R
Burch, Tanya
Ly, Valentina
Hatch, Grant M
Zelinski, Teresa
spellingShingle Elliott, Alison M
Simard, Louise R
Coghlan, Gail
Chudley, Albert E
Chodirker, Bernard N
Greenberg, Cheryl R
Burch, Tanya
Ly, Valentina
Hatch, Grant M
Zelinski, Teresa
A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort
author_facet Elliott, Alison M
Simard, Louise R
Coghlan, Gail
Chudley, Albert E
Chodirker, Bernard N
Greenberg, Cheryl R
Burch, Tanya
Ly, Valentina
Hatch, Grant M
Zelinski, Teresa
author_sort Elliott, Alison M
title A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort
title_short A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort
title_full A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort
title_fullStr A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort
title_full_unstemmed A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort
title_sort novel mutation in kiaa0196: identification of a gene involved in ritscher–schinzel/3c syndrome in a first nations cohort
publisher BMJ
publishDate 2013
url http://dx.doi.org/10.1136/jmedgenet-2013-101715
https://syndication.highwire.org/content/doi/10.1136/jmedgenet-2013-101715
genre First Nations
genre_facet First Nations
op_source Journal of Medical Genetics
volume 50, issue 12, page 819-822
ISSN 0022-2593 1468-6244
op_doi https://doi.org/10.1136/jmedgenet-2013-101715
container_title Journal of Medical Genetics
container_volume 50
container_issue 12
container_start_page 819
op_container_end_page 822
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