Haga su diagnóstico
Tau, Cristina; Viterbo, Gisela; Geniuk, Nadia.
Med. infant
; 15(4): 361-363, dic. 2008. ilus
Artículo en Español | LILACS | ID: lil-541269
Documentos relacionados
A kilonova following a long-duration gamma-ray burst at 350 Mpc.
[Clinical and molecular genetic analysis of a child with Schmid type metaphyseal chondrodysplasia].
Leucine improves thiram-induced tibial dyschondroplasia and gut microbiota dysbiosis in broilers.
Rare Variant of PTH1R Mutation in an Indian Family.
Spondyloepimetaphyseal dysplasia-Maroteaux type due to dominant TRPV4 mutation: expanding the phenotype with a case report.
Schwartz Jampel Syndrome (SJS)-One in a Million Syndrome.
A scoping review of nutrition issues and management strategies in individuals with skeletal dysplasia.
Five siblings expand the spectrum of GPC6-related skeletal dysplasia.
Antenatal diagnostic dilemma in a pseudodominant pedigree with lamin-B receptor (LBR)-related regressive spondylometaphyseal dysplasia.
Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorption.