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ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE

Known as: AMDM 
 
National Institutes of Health

Papers overview

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2019
2019
Analytical solutions describing free transverse vibrations with large amplitude of axially loaded Euler–Bernoulli beams for… Expand
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2016
2016
We obtain analytical expressions, both in terms of parametric integrals and Passarino–Veltman scalar functions, for the one-loop… Expand
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2015
2015
Acromesomelic dysplasia Maroteaux type (AMDM) is an autosomal recessive skeletal disorder characterized by disproportionate short… Expand
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2015
2015
CONTEXT C-type natriuretic peptide (CNP) is a crucial regulator of endochondral bone growth. In a previous report of a child with… Expand
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2015
2015
  • QiboMao
  • 2015
  • Corpus ID: 55708856
The Adomian modified decomposition method (AMDM) is employed in this paper for dynamic analysis of a rotating EulerBernoulli beam… Expand
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2014
2014
BackgroundThe cn/cn dwarf mouse is caused by a loss-of-function mutation in the natriuretic peptide receptor 2 (NPR-2) gene which… Expand
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2008
2008
AMDM, a form of osteochondrodysplasia, is due to the loss-of-function mutations in NPR-B gene. This study investigated the… Expand
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Highly Cited
2006
Highly Cited
2006
CONTEXT C-type natriuretic peptide (CNP) is an important regulator of skeletal growth. Loss-of-function mutations affecting the… Expand
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2000
2000
Acromesomelic dysplasia Maroteaux type (AMDM) is an autosomal recessive disorder belonging to the group of acromesomelic… Expand
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1998
1998
Acromesomelic dysplasias are skeletal disorders that disproportionately affect the middle and distal segments of the appendicular… Expand
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