Children with growth hormone deficiency and Chiari I malformation: a morphometric analysis of the posterior cranial fossa.
about
Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.Cerebrospinal fluid hydrodynamics in type I Chiari malformation.The human occipital bone: review and update on its embryology and molecular development.Diameters and bone thickness at the margin of the foramen magnum in dry skulls from pediatric population: a cross-sectional anatomical study.Human Foramen Magnum Area and Posterior Cranial Fossa Volume Growth in Relation to Cranial Base Synchondrosis Closure in the Course of Child Development.Growth hormone deficiency in a case of crouzon syndrome with hydrocephalus.The Association of Pseudohypoparathyroidism Type Ia with Chiari Malformation Type I: A Coincidence or a Common Link?Histological study of the occipital bone from patients with Chiari I malformation.Skull base morphology in fibroblast growth factor receptor type 2-related faciocraniosynostosis: a descriptive analysis.
P2860
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P2860
Children with growth hormone deficiency and Chiari I malformation: a morphometric analysis of the posterior cranial fossa.
description
2003 nî lūn-bûn
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name
Children with growth hormone d ...... f the posterior cranial fossa.
@en
Children with growth hormone d ...... f the posterior cranial fossa.
@nl
type
label
Children with growth hormone d ...... f the posterior cranial fossa.
@en
Children with growth hormone d ...... f the posterior cranial fossa.
@nl
prefLabel
Children with growth hormone d ...... f the posterior cranial fossa.
@en
Children with growth hormone d ...... f the posterior cranial fossa.
@nl
P2093
P356
P1476
Children with growth hormone d ...... f the posterior cranial fossa.
@en
P2093
Alfred A Bartolucci
Jeffrey P Blount
John C Wellons
Matthew D Smyth
Paul A Grabb
R Shane Tubbs
W Jerry Oakes
P304
P356
10.1159/000070416
P577
2003-06-01T00:00:00Z