Genetics of congenital hypogonadotropic hypogonadism in Denmark.
about
Tooth agenesis and orofacial clefting: genetic brothers in arms?Hypogonadotropic Hypogonadism due to Novel FGFR1 MutationsDominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome.GnRH receptor gene mutations in adolescents and young adults presenting with signs of partial gonadotropin deficiency.The Use of Variant Maps to Explore Domain-Specific Mutations of FGFR1.Childhood growth in boys with congenital hypogonadotropic hypogonadism.Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.Isolated GNRH deficiency: genotypic and phenotypic characteristics of the genetically heterogeneous Greek population.
P2860
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P2860
Genetics of congenital hypogonadotropic hypogonadism in Denmark.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年學術文章
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name
Genetics of congenital hypogonadotropic hypogonadism in Denmark.
@en
Genetics of congenital hypogonadotropic hypogonadism in Denmark.
@nl
type
label
Genetics of congenital hypogonadotropic hypogonadism in Denmark.
@en
Genetics of congenital hypogonadotropic hypogonadism in Denmark.
@nl
prefLabel
Genetics of congenital hypogonadotropic hypogonadism in Denmark.
@en
Genetics of congenital hypogonadotropic hypogonadism in Denmark.
@nl
P2093
P50
P1476
Genetics of congenital hypogonadotropic hypogonadism in Denmark.
@en
P2093
Jacob Gerner Lawaetz
Johanna Känsäkoski
Peter Christiansen
P304
P356
10.1016/J.EJMG.2014.04.002
P577
2014-04-13T00:00:00Z