The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions.
about
Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromesA new pathway in the control of the initiation of puberty: the MKRN3 geneThe role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutationsExpanding the phenotype and genotype of female GnRH deficiencyThe Dlx5 and Foxg1 transcription factors, linked via miRNA-9 and -200, are required for the development of the olfactory and GnRH system.Uncovering novel reproductive defects in neurokinin B receptor null mice: closing the gap between mice and men.Profiling, Bioinformatic, and Functional Data on the Developing Olfactory/GnRH System Reveal Cellular and Molecular Pathways Essential for This Process and Potentially Relevant for the Kallmann Syndrome.Central precocious puberty caused by mutations in the imprinted gene MKRN3.The consequences of mutations in the reproductive endocrine system.Incidence, phenotypic features and molecular genetics of Kallmann syndrome in Finland.Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experienceGenetic Overlap between Holoprosencephaly and Kallmann Syndrome.A comprehensive review of genetics and genetic testing in azoospermia.The Novel Actions of the Metabolite GnRH-(1-5) are Mediated by a G Protein-Coupled Receptor.Mutation analyses in pedigrees and sporadic cases of ethnic Han Chinese Kallmann syndrome patients.New understandings of the genetic basis of isolated idiopathic central hypogonadism.Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1.The Genetics of Infertility: Current Status of the Field.Pubertal development and regulation.Renal agenesis in Kallmann syndrome: a network approach.Fertility and fragrance: another cause of Kallmann syndrome.Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism.Hypogonadotropic hypogonadism in a trisomy X carrier: phenotype description and genotype correlation.Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated families.Expanding the genetic spectrum of ANOS1 mutations in patients with congenital hypogonadotropic hypogonadism.[Male infertility: recent developments].New Insights Into the Long Non-coding RNA SRA: Physiological Functions and Mechanisms of Action
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The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
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scientific article published on 29 August 2009
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vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions.
@en
The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions.
@nl
type
label
The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions.
@en
The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions.
@nl
prefLabel
The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions.
@en
The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions.
@nl
P1476
The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions.
@en
P2093
A Kemal Topaloglu
P304
P356
10.1111/J.1365-2265.2009.03687.X
P577
2009-08-29T00:00:00Z