A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort
Published in: | Journal of Medical Genetics |
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Main Authors: | , , , , , , , , , |
Format: | Article in Journal/Newspaper |
Language: | English |
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BMJ
2013
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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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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 |
_version_ |
1810443842066841600 |