Found: 4
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Duplication 2p25 in a child with clinical features of CHARGE syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 5, p. 1148, doi. 10.1002/ajmg.a.37592
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- Publication type:
- Article
The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development.
- Published in:
- Developmental Dynamics, 2014, v. 243, n. 9, p. 1055, doi. 10.1002/dvdy.24156
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- Publication type:
- Article
Single Cell Transcriptomics Reveal Abnormalities in Neurosensory Patterning of the Chd7 Mutant Mouse Ear.
- Published in:
- Frontiers in Genetics, 2018, p. N.PAG, doi. 10.3389/fgene.2018.00473
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- Publication type:
- Article
CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 2, p. 434, doi. 10.1093/hmg/ddt435
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- Publication type:
- Article