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Terminal 10q26.12 deletion is associated with neonatal asymmetric crying facies syndrome: a case report and literature review
BACKGROUND: The terminal 10q26 deletion syndrome is a clinically heterogeneous disorder without identified genotype–phenotype correlations. We reported a case of congenital asymmetric crying facies (ACF) syndrome with 10q26.12qter deletion and discussed their genotype–phenotype correlations and the...
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| Publicado no: | Mol Cytogenet |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8278754/ https://ncbi.nlm.nih.gov/pubmed/34256807 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-021-00554-1 |
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