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MYO1H gene

Known as: FLJ37587, MYO1H, MYOSIN IH 
 
National Institutes of Health

Papers overview

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2019
2019
OBJECTIVE This study aimed to evaluate the association of genetic variants inACTN3 and MYO1H with craniofacial skeletal patterns… Expand
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2018
2018
Mandibular prognathism (MP) is regarded as a craniofacial deformity resulting from the combined effects of environmental and… Expand
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2017
2017
Background Congenital central hypoventilation syndrome (CCHS) is a rare life-threatening disorder of respiratory and autonomic… Expand
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2017
2017
Introduction: Our goal was to verify the association between candidate polymorphisms and skeletal Class III malocclusion in a… Expand
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2016
2016
INTRODUCTION Mandibular retrognathism may be the result of a developmental abnormality or the unfavorable positional relationship… Expand
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2015
2015
This study evaluated associations between craniofacial candidate genes and skeletal variation in patients with malocclusion… Expand
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2013
2013
Background. The Matrilin-1 gene is thought to be involved in the formation of the filamentous network of the cartilage's… Expand
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2012
2012
INTRODUCTION Several candidate loci have been suggested as influencing mandibular prognathism (1p22.1, 1p22.2, 1p36, 3q26.2, 5p13… Expand
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2009
2009
Objective:Hereditary spastic paraplegias (HSP) are genetically exceedingly heterogeneous. To date, 37 genetic loci for HSP have… Expand
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2002
2002
Myosin isozymes are essential for hair cells, the sensory cells of the inner ear. Because a myosin-I subfamily member may mediate… Expand
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