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Mouse and Human CRKL Is Dosage Sensitive for Cardiac Outflow Tract Formation
The human chromosome 22q11.2 region is susceptible to rearrangements during meiosis leading to velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome (22q11DS) characterized by conotruncal heart defects (CTDs) and other congenital anomalies. The majority of individuals have a 3 Mb deletion whose prox...
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| Gepubliceerd in: | Am J Hum Genet |
|---|---|
| Hoofdauteurs: | , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Elsevier
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4320261/ https://ncbi.nlm.nih.gov/pubmed/25658046 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2014.12.025 |
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