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Gracile bone dysplasia

Known as: Habrodysplasia, SKELETAL DYSPLASIA, LETHAL, WITH GRACILE BONES, OSTEOCRANIOSPLENIC SYNDROME 
National Institutes of Health

Papers overview

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2018
2018
SV40 has served as a powerful tool for understanding fundamental viral and cellular processes; however, despite extensive study… Expand
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2015
2015
The syndrome of hypoparathyroidism, retardation (of growth and mental development) with dysmorphic features, HRD syndrome, also… Expand
2014
2014
To the Editor : Kenny–Caffey syndrome (KCS) is a rare condition associated with short stature, cortical thickening of tubular… Expand
Highly Cited
2013
Highly Cited
2013
Kenny-Caffey syndrome (KCS) and the similar but more severe osteocraniostenosis (OCS) are genetic conditions characterized by… Expand
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2011
2011
To study the chemical constituents from the stems and leaves of Lophatherum gracile Brongn,the compounds were isolated by column… Expand
2006
2006
Osteocraniostenosis is a severe skeletal dysplasia characterized by a hypomineralized skull that has been previously described as… Expand
2005
2005
We report on two brothers with ossification anomalies of membranous and cranial bones, remodeling defect of long bones leading to… Expand
2002
2002
Abstract. Gracile bone dysplasias constitute a group of disorders characterised by extremely slender bones with or without… Expand
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2002
2002
Objective To study the chemical constituents of Lophatherum gracile Brongn.Methods Separation by the chromatographic methods… Expand
1997
1997
  • A. Verloes
  • American journal of medical genetics
  • 1997
  • Corpus ID: 42615713