Lataa...
Mild phenotypic manifestation of a 7p15.3p21.2 deletion.
A 28 month old girl with dysmorphic features was found to have an interstitial deletion of the short arm of chromosome 7p15.3-7p21.2. The patient had ptosis, dacryostenosis, pectus excavatum, short hands, and her development was normal or mildly delayed. Craniosynostosis and growth retardation, whic...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
1993
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1016466/ https://ncbi.nlm.nih.gov/pubmed/8411039 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|