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Chromosome 22q11.21 and 11p15.4 microdeletions confirmed by high‐throughput sequencing analysis in one patient with asymmetric cry syndrome: Case report and review of the literature
Healthcare providers treating newborns with asymmetric cry syndrome should consider 22q11.2 microdeletion within the differential diagnosis list and order appropriate genetic testing.
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| Publicado en: | Clin Case Rep |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2021
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8142403/ https://ncbi.nlm.nih.gov/pubmed/34084494 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.4072 |
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