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MYO1H gene

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
OBJECTIVE This study aimed to evaluate the association of genetic variants inACTN3 and MYO1H with craniofacial skeletal patterns… Expand
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
Introduction: Our goal was to verify the association between candidate polymorphisms and skeletal Class III malocclusion in a… Expand
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2017
2017
Background Congenital central hypoventilation syndrome (CCHS) is a rare life-threatening disorder of respiratory and autonomic… Expand
Review
2017
Review
2017
Mandibular prognathism is defined as an abnormal forward projection of the mandible beyond the standard relation to the cranial… Expand
2016
2016
INTRODUCTION Mandibular retrognathism may be the result of a developmental abnormality or the unfavorable positional relationship… Expand
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Highly Cited
2015
Highly Cited
2015
This study evaluated associations between craniofacial candidate genes and skeletal variation in patients with malocclusion… Expand
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Highly Cited
2012
Highly Cited
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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Highly Cited
2002
Highly Cited
2002
Myosin isozymes are essential for hair cells, the sensory cells of the inner ear. Because a myosin-I subfamily member may mediate… Expand