Skip Nav Destination
Close Modal
Update search
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
NARROW
Format
Journal
Article Type
TOC Section
Date
Availability
1-2 of 2
Keywords: 22q11.2 deletion syndrome
Close
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Sort by
Journal Articles
Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx
Journal:
Development
Development (2020) 147 (3): dev185256.
Published: 3 February 2020
..., in a distribution established in the early embryo. We further show that biallelic expression of the CPM regulatory gene Tbx1 , haploinsufficient in 22q11.2 deletion syndrome patients, is required for the correct patterning of muscles with CPM-derived connective tissue. Our results suggest that CPM plays...
Includes: Supplementary data
Journal Articles
Journal:
Development
Development (2004) 131 (21): 5491–5502.
Published: 1 November 2004
... with del22q11. † Author for correspondence (e-mail: deepak.srivastava@utsouthwestern.edu ) * These authors contributed equally to this work 13 8 2004 © 2004. 2004 Tbx1 22q11.2 deletion syndrome Anterior heart field Foxa2 Fgf8 Fgf10 Human chromosomal deletion...
