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Low size for selective and idiopathic growth hormone deficiency associated with Crouzon SyndromeBaja talla por déficit selectivo e idiopático de hormona de crecimiento asociado al Síndrome de Crouzon
(Intituto Tecnológico de Santo Domingo (INTEC), 2017)
Q289P mutation in FGFR2 gene causes Saethre-Chotzen syndrome: Some considerations about familial heterogeneity
(Alliance Communications Group Division Allen PressLawrenceEUA, 2006)
Apert syndrome: Analysis of associated brain malformations and conformational changes determined by surgical treatment
(2004-03-01)
Apert Syndrome, also called acrocephalosyndactylia type 1, is characterized by craniostenosis with early fusion of sutures of the vault and/ or cranial base, associated to mid-face hypoplasia, symmetric syndactylia of the ...
Apert syndrome: Factors involved in the cognitive development
(2005-12-01)
Apert syndrome is characterized by craniosynostosis, symmetric syndactyly and other systemic malformations, with mental retardation usually present. The objective of this study was to correlate brain malformations and ...
Apert syndrome: Analysis of associated brain malformations and conformational changes determined by surgical treatment
(2004-03-01)
Apert Syndrome, also called acrocephalosyndactylia type 1, is characterized by craniostenosis with early fusion of sutures of the vault and/ or cranial base, associated to mid-face hypoplasia, symmetric syndactylia of the ...