A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene.
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An update on the genetic causes of central precocious pubertyThe first Japanese case of central precocious puberty with a novel MKRN3 mutation.DNA Methylation Patterns in the Hypothalamus of Female Pubertal GoatsTime Course of Central Precocious Puberty Development Caused by an MKRN3 Gene Mutation: A Prismatic Case.MKRN3 levels in girls with central precocious puberty and correlation with sexual hormone levels: a pilot study.Clinical Exome Sequencing Reveals MKRN3 Pathogenic Variants in Familial and Nonfamilial Idiopathic Central Precocious Puberty.Two Frameshift Mutations in MKRN3 in Turkish Patients with Familial Central Precocious Puberty.The tempo of human childhood: a maternal foot on the accelerator, a paternal foot on the brake.
P2860
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P2860
A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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name
A case of familial central pre ...... in RING finger protein 3 gene.
@ast
A case of familial central pre ...... in RING finger protein 3 gene.
@en
type
label
A case of familial central pre ...... in RING finger protein 3 gene.
@ast
A case of familial central pre ...... in RING finger protein 3 gene.
@en
prefLabel
A case of familial central pre ...... in RING finger protein 3 gene.
@ast
A case of familial central pre ...... in RING finger protein 3 gene.
@en
P2093
P2860
P50
P1476
A case of familial central pre ...... rin RING finger protein 3 gene
@en
P2093
Caterina Luongo
Emanuele Miraglia del Giudice
Grazia Cantelmi
Grazia Cirillo
P2860
P2888
P356
10.1186/S12902-015-0056-8
P577
2015-10-23T00:00:00Z