Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland

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http://hdl.handle.net/10138/162343

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Laitinen , E-M , Vaaralahti , K , Tommiska , J , Eklund , E , Tervaniemi , M , Valanne , L & Raivio , T 2011 , ' Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland ' , Orphanet journal of rare diseases , vol. 6 , pp. 41 . https://doi.org/10.1186/1750-1172-6-41

Title: Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland
Author: Laitinen, Eeva-Maria; Vaaralahti, Kirsi; Tommiska, Johanna; Eklund, Elina; Tervaniemi, Mari; Valanne, Leena; Raivio, Taneli
Contributor: University of Helsinki, Department of Physiology
University of Helsinki, Medicum
University of Helsinki, Laboratory Animal Centre
University of Helsinki, Medicum
University of Helsinki, Department of Diagnostics and Therapeutics
University of Helsinki, Department of Physiology
Date: 2011
Language: eng
Number of pages: 10
Belongs to series: Orphanet journal of rare diseases
ISSN: 1750-1172
URI: http://hdl.handle.net/10138/162343
Subject: IDIOPATHIC HYPOGONADOTROPIC HYPOGONADISM
GONADOTROPIN-RELEASING-HORMONE
GROWTH-FACTOR RECEPTOR-1
OF-FUNCTION MUTATIONS
CHARGE SYNDROME
DELAYED PUBERTY
PROTEIN
DEFICIENCY
GENES
CHD7
1184 Genetics, developmental biology, physiology
3111 Biomedicine
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