A new interstitial deletion of 4q (q21.1::q22.1).
A unique case of de novo interstitial deletion of chromosome 4 is described involving loss of band q21. The male newborn had multiple abnormalities including frontal bossing, prominent occiput, low set ears, micrognathia, short sternum, short, broad hands and feet, agenesis of the corpus callosum, a...
Guardat en:
| Publicat a: | J Med Genet |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Publishing Group
1989
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015717/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2585461/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.26.10.644 |
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