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

Eeva-Maria Laitinen, Kirsi Vaaralahti, Johanna Tommiska, Elina Eklund, Mari Tervaniemi, Leena Valanne, Taneli Raivio

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalOrphanet journal of rare diseases
Volume6
Pages (from-to)41
Number of pages10
ISSN1750-1172
DOIs
Publication statusPublished - 2011
MoE publication typeA1 Journal article-refereed

Fields of Science

  • 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

Cite this

@article{9a35b0f85755457c8c2c172a3b5b6a26,
title = "Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland",
keywords = "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",
author = "Eeva-Maria Laitinen and Kirsi Vaaralahti and Johanna Tommiska and Elina Eklund and Mari Tervaniemi and Leena Valanne and Taneli Raivio",
year = "2011",
doi = "10.1186/1750-1172-6-41",
language = "English",
volume = "6",
pages = "41",
journal = "Orphanet journal of rare diseases",
issn = "1750-1172",
publisher = "BMC",

}

Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland. / Laitinen, Eeva-Maria; Vaaralahti, Kirsi; Tommiska, Johanna; Eklund, Elina; Tervaniemi, Mari; Valanne, Leena; Raivio, Taneli.

In: Orphanet journal of rare diseases, Vol. 6, 2011, p. 41.

Research output: Contribution to journalArticleScientificpeer-review

TY - JOUR

T1 - Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland

AU - Laitinen, Eeva-Maria

AU - Vaaralahti, Kirsi

AU - Tommiska, Johanna

AU - Eklund, Elina

AU - Tervaniemi, Mari

AU - Valanne, Leena

AU - Raivio, Taneli

PY - 2011

Y1 - 2011

KW - IDIOPATHIC HYPOGONADOTROPIC HYPOGONADISM

KW - GONADOTROPIN-RELEASING-HORMONE

KW - GROWTH-FACTOR RECEPTOR-1

KW - OF-FUNCTION MUTATIONS

KW - CHARGE SYNDROME

KW - DELAYED PUBERTY

KW - PROTEIN

KW - DEFICIENCY

KW - GENES

KW - CHD7

KW - 1184 Genetics, developmental biology, physiology

KW - 3111 Biomedicine

U2 - 10.1186/1750-1172-6-41

DO - 10.1186/1750-1172-6-41

M3 - Article

VL - 6

SP - 41

JO - Orphanet journal of rare diseases

JF - Orphanet journal of rare diseases

SN - 1750-1172

ER -