Growth Hormone Receptor Mutations Related to Individual Dwarfism.

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Term Occurence Count Dictionary
Laron syndrome 2 endocrinologydiseases
osteoporosis 1 endocrinologydiseases

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Laron syndrome 1780 process in the dwarf phenotype. Until now, more than 90 GHR mutations relevant to human short stature ( Laron syndrome and idiopathic short stature), including deletions, missense, nonsense, frameshift, and splice site
Laron syndrome 4470 and sheep [[17]], and sex-linked dwarfism (SLD) occurs in chicken [[2],[18],[19],[20]]. For example, Laron syndrome (LS), also known as growth hormone insensitivity syndrome, and idiopathic short stature (ISS) are autosomal
osteoporosis 4118 short. They also have decreased bone mineral density and increased adiposity, with a greater risk of osteoporosis , lipid disorders, and cardiovascular disease [[9]].Dwarfism is characterized by normal or elevated serum

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