Laddar...
Eye Abnormalities in Fryns Syndrome
Fryns syndrome is a rare, generally lethal, autosomal recessive multiple congenital anomaly (MCA) syndrome first described in 1979. Patients with the syndrome present with the classical findings of cloudy cornea, brainmalformations, diaphragmaticdefects, and distal limb deformities. Over 70 patients...
Sparad:
| I publikationen: | Am J Med Genet A |
|---|---|
| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2004
|
| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6719310/ https://ncbi.nlm.nih.gov/pubmed/14994236 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.20520 |
| Taggar: |
Lägg till en tagg
Inga taggar, Lägg till första taggen!
|