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Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature
BACKGROUND: Terminal deletions of chromosome 4q are associated with a broad spectrum of phenotypes including cardiac, craniofacial, digital, and cognitive impairment. The rarity of this syndrome renders genotype-phenotype correlation difficult, which is further complicated by the widely different ph...
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| Hauptverfasser: | , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2014
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4077152/ https://ncbi.nlm.nih.gov/pubmed/24962056 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-15-72 |
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