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Understanding the Role of Tbx1 as a Candidate Gene for 22q11.2 Deletion Syndrome
22q11.2 deletion syndrome (22q11.2DS) is caused by a commonly occurring microdeletion on chromosome 22. Clinical findings include cardiac malformations, thymic and parathyroid hypoplasia, craniofacial dysmorphisms, and dental defects. These phenotypes are due mainly to abnormal development of the ph...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3840116/ https://ncbi.nlm.nih.gov/pubmed/23996541 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11882-013-0384-6 |
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