Cargando…
Fryns syndrome: a case associated with kryotype XO
Autores principales: | Dawani, Nader M.H., Al Madhoob, Abdul Raoof, Ali, Fuad Abdulla, Shabib, Fatima |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
King Faisal Specialist Hospital and Research Centre
2004
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147895/ https://www.ncbi.nlm.nih.gov/pubmed/15323276 http://dx.doi.org/10.5144/0256-4947.2004.129 |
Ejemplares similares
-
Challenging Anaesthesia Management of a Patient with Fryns Syndrome: A Case Report
por: Kaya, Celal, et al.
Publicado: (2023) -
Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
por: Van Buggenhout, Griet, et al.
Publicado: (2006) -
Diaphragmatic Hernia as a Prenatal Feature of Glycosylphosphatidylinositol Biosynthesis Defects and the Overlap With Fryns Syndrome – Literature Review
por: Kosinski, Przemyslaw, et al.
Publicado: (2021) -
Lujan–Fryns Syndrome (LFS): A Unique Combination of Hypernasality, Marfanoid Body Habitus, and Neuropsychiatric Issues, Presenting as Acute-Onset Dysphagia
por: Khan, Abidullah, et al.
Publicado: (2016) -
NeXO Web: the NeXO ontology database and visualization platform
por: Dutkowski, Janusz, et al.
Publicado: (2014)