Cargando…
Criteria of radiological diagnosis for neonates with hypochondroplasia
Autores principales: | Nagasaki, Keisuke, Saito, Tomoko, Takagi, Masaki, Hasegawa, Tomonobu, Nishimura, Gen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428262/ http://dx.doi.org/10.1186/1687-9856-2015-S1-O24 |
Ejemplares similares
-
A Japanese familial case of hypochondroplasia with a novel mutation in
FGFR3
por: Nagahara, Keiko, et al.
Publicado: (2016) -
A study of the etiology of transient congenital hypothyroidism in Niigata Prefecture, Japan
por: Nagasaki, Keisuke, et al.
Publicado: (2013) -
Failure to diagnose hypochondroplasia by prenatal diagnosis: a case report
por: Xie, Hua, et al.
Publicado: (2023) -
Extensive Limb Lengthening for Achondroplasia and Hypochondroplasia
por: Paley, Dror
Publicado: (2021) -
Osteogenesis imperfecta IIC caused by a novel heterozygous mutation in the C-propeptide region of COL1A1
por: Takagi, Masaki, et al.
Publicado: (2014)