Laddar...
Diaphragmatic Hernia as a Prenatal Feature of Glycosylphosphatidylinositol Biosynthesis Defects and the Overlap With Fryns Syndrome – Literature Review
Fryns syndrome is an autosomal recessive multiple congenital anomaly syndrome, with diaphragmatic defects and secondary lung hypoplasia as cardinal features. Despite it was reported first in 1979, its exact etiology has not been established to date. With this review, we would like to draw attention...
Sparad:
| I publikationen: | Front Genet |
|---|---|
| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Frontiers Media S.A.
2021
|
| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8215573/ https://ncbi.nlm.nih.gov/pubmed/34163527 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.674722 |
| Taggar: |
Lägg till en tagg
Inga taggar, Lägg till första taggen!
|