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58461.
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58462.
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58463.
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58464.
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58465.
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30-day readmission for patients undergoing percutaneous coronary interventions in New York state. [electronic resource] by
- Hannan, Edward L
- Zhong, Ye
- Krumholz, Harlan
- Walford, Gary
- Holmes, David R
- Stamato, Nicholas J
- Jacobs, Alice K
- Venditti, Ferdinand J
- Sharma, Samin
- King, Spencer B
Producer: 20120423
In:
JACC. Cardiovascular interventions vol. 4
Availability: No items available.
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58466.
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58467.
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58468.
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58469.
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58470.
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58471.
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58472.
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58473.
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58474.
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58475.
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58476.
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58477.
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TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone. [electronic resource] by
- Huang, Lijia
- Szymanska, Katarzyna
- Jensen, Victor L
- Janecke, Andreas R
- Innes, A Micheil
- Davis, Erica E
- Frosk, Patrick
- Li, Chunmei
- Willer, Jason R
- Chodirker, Bernard N
- Greenberg, Cheryl R
- McLeod, D Ross
- Bernier, Francois P
- Chudley, Albert E
- Müller, Thomas
- Shboul, Mohammad
- Logan, Clare V
- Loucks, Catrina M
- Beaulieu, Chandree L
- Bowie, Rachel V
- Bell, Sandra M
- Adkins, Jonathan
- Zuniga, Freddi I
- Ross, Kevin D
- Wang, Jian
- Ban, Matthew R
- Becker, Christian
- Nürnberg, Peter
- Douglas, Stuart
- Craft, Cheryl M
- Akimenko, Marie-Andree
- Hegele, Robert A
- Ober, Carole
- Utermann, Gerd
- Bolz, Hanno J
- Bulman, Dennis E
- Katsanis, Nicholas
- Blacque, Oliver E
- Doherty, Dan
- Parboosingh, Jillian S
- Leroux, Michel R
- Johnson, Colin A
- Boycott, Kym M
Producer: 20120202
In:
American journal of human genetics vol. 89
Availability: No items available.
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58478.
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Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type. [electronic resource] by
- Min, Byung-Joo
- Kim, Namshin
- Chung, Taesu
- Kim, Ok-Hwa
- Nishimura, Gen
- Chung, Chin Youb
- Song, Hae Ryong
- Kim, Hyun Woo
- Lee, Hye Ran
- Kim, Jiwoong
- Kang, Tae-Hoon
- Seo, Myung-Eui
- Yang, San-Deok
- Kim, Do-Hwan
- Lee, Seung-Bok
- Kim, Jong-Il
- Seo, Jeong-Sun
- Choi, Ji-Yeob
- Kang, Daehee
- Kim, Dongsup
- Park, Woong-Yang
- Cho, Tae-Joon
Producer: 20120202
In:
American journal of human genetics vol. 89
Availability: No items available.
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58479.
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Disruption of teashirt zinc finger homeobox 1 is associated with congenital aural atresia in humans. [electronic resource] by
- Feenstra, Ilse
- Vissers, Lisenka E L M
- Pennings, Ronald J E
- Nillessen, Willy
- Pfundt, Rolph
- Kunst, Henricus P
- Admiraal, Ronald J
- Veltman, Joris A
- van Ravenswaaij-Arts, Conny M A
- Brunner, Han G
- Cremers, Cor W R J
Producer: 20120202
In:
American journal of human genetics vol. 89
Availability: No items available.
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58480.
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