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In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
BACKGROUND: 22q11.2 deletion syndrome (22q11DS), a copy number variation (CNV) disorder, occurs in approximately 1:4000 live births due to a heterozygous microdeletion at position 11.2 (proximal) on the q arm of human chromosome 22 (hChr22) (McDonald-McGinn and Sullivan, Medicine 90:1-18, 2011). Thi...
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| Publicado no: | J Neurodev Disord |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6554986/ https://ncbi.nlm.nih.gov/pubmed/31174463 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-019-9267-z |
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