Results
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5381.
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Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability. [electronic resource] by
- Maduro, Valerie
- Pusey, Barbara N
- Cherukuri, Praveen F
- Atkins, Paul
- du Souich, Christèle
- Rupps, Rosemarie
- Limbos, Marjolaine
- Adams, David R
- Bhatt, Samarth S
- Eydoux, Patrice
- Links, Amanda E
- Lehman, Anna
- Malicdan, May C
- Mason, Christopher E
- Morimoto, Marie
- Mullikin, James C
- Sear, Andrew
- Van Karnebeek, Clara
- Stankiewicz, Pawel
- Gahl, William A
- Toro, Camilo
- Boerkoel, Cornelius F
Producer: 20171107
In:
Orphanet journal of rare diseases vol. 11
Availability: No items available.
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5382.
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5383.
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5384.
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5385.
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5386.
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5387.
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5388.
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5389.
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5390.
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5391.
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Spontaneous hyperventilation and brain tissue hypoxia in patients with severe brain injury. [electronic resource] by
- Carrera, Emmanuel
- Schmidt, J Michael
- Fernandez, Luis
- Kurtz, Pedro
- Merkow, Maxwell
- Stuart, Morgan
- Lee, Kiwon
- Claassen, Jan
- Sander Connolly, E
- Mayer, Stephan A
- Badjatia, Neeraj
Producer: 20100709
In:
Journal of neurology, neurosurgery, and psychiatry vol. 81
Availability: No items available.
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5392.
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5393.
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Transcription factor 4 and myocyte enhancer factor 2C mutations are not common causes of Rett syndrome. [electronic resource] by
- Armani, Roksana
- Archer, Hayley
- Clarke, Angus
- Vasudevan, Pradeep
- Zweier, Christiane
- Ho, Gladys
- Williamson, Sarah
- Cloosterman, Desiree
- Yang, Nan
- Christodoulou, John
Producer: 20120730
In:
American journal of medical genetics. Part A vol. 158A
Availability: No items available.
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5394.
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5395.
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5396.
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5397.
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5398.
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5399.
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5400.
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