Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory.
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A Jacob/Nsmf Gene Knockout Results in Hippocampal Dysplasia and Impaired BDNF Signaling in Dendritogenesis.Identifying the unmet health needs of patients with congenital hypogonadotropic hypogonadism using a web-based needs assessment: implications for online interventions and peer-to-peer supportTwo families with normosmic congenital hypogonadotropic hypogonadism and biallelic mutations in KISS1R (KISS1 receptor): clinical evaluation and molecular characterization of a novel mutationBiochemical and MRI findings of Kallmann's syndrome.Erythrocyte membrane antigen frequencies in patients with Type II congenital smell loss.Mutations in KISS1 are not responsible for idiopathic hypogonadotropic hypogonadism in Chinese patients.Psychosexual development in men with congenital hypogonadotropic hypogonadism on long-term treatment: a mixed methods study.Unique phenotype in a patient with CHARGE syndrome.Fibroblast growth factor signaling deficiencies impact female reproduction and kisspeptin neurons in miceMolecular basis for the Kallmann syndrome-linked fibroblast growth factor receptor mutation.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.Semaphorin signaling in the development and function of the gonadotropin hormone-releasing hormone system.Living with Kallmann Syndrome - Analysis of Subjective Experience Reports from Women.Human pheromones and food odors: epigenetic influences on the socioaffective nature of evolved behaviorsInvertebrate models of kallmann syndrome: molecular pathogenesis and new disease genes.Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal lifeThe terminal nerve plays a prominent role in GnRH-1 neuronal migration independent from proper olfactory and vomeronasal connections to the olfactory bulbs.Clinical characteristics of 138 Chinese female patients with idiopathic hypogonadotropic hypogonadism.Olfactory loss and dysfunction in ciliopathies: Molecular mechanisms and potential therapies.Congenital Hypogonadotropic Hypogonadism and Constitutional Delay of Growth and Puberty Have Distinct Genetic Architectures.Next-generation sequencing of patients with congenital anosmia.Clinical data and genetic mutation in Kallmann syndrome with CHARGE syndrome: Case report and pedigree analysis
P2860
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P2860
Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory.
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Genetic basis and variable phe ...... me: towards a unifying theory.
@ast
Genetic basis and variable phe ...... me: towards a unifying theory.
@en
Genetic basis and variable phe ...... me: towards a unifying theory.
@nl
type
label
Genetic basis and variable phe ...... me: towards a unifying theory.
@ast
Genetic basis and variable phe ...... me: towards a unifying theory.
@en
Genetic basis and variable phe ...... me: towards a unifying theory.
@nl
prefLabel
Genetic basis and variable phe ...... me: towards a unifying theory.
@ast
Genetic basis and variable phe ...... me: towards a unifying theory.
@en
Genetic basis and variable phe ...... me: towards a unifying theory.
@nl
P50
P1476
Genetic basis and variable phe ...... ome: towards a unifying theory
@en
P2093
Richard Quinton
P304
P356
10.1016/J.TEM.2011.03.002
P577
2011-04-20T00:00:00Z