Evaluation of SHOX copy number variations in patients with Mullerian aplasia

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Sandbacka , M , Halttunen , M , Jokimaa , V , Aittomäki , K & Laivuori , H 2011 , ' Evaluation of SHOX copy number variations in patients with Mullerian aplasia ' , Orphanet journal of rare diseases , vol. 6 , 53 . https://doi.org/10.1186/1750-1172-6-53

Title: Evaluation of SHOX copy number variations in patients with Mullerian aplasia
Author: Sandbacka, Maria; Halttunen, Mervi; Jokimaa, Varpu; Aittomäki, Kristiina; Laivuori, Hannele
Contributor organization: Department of Medical and Clinical Genetics
Department of Obstetrics and Gynecology
Genome-Scale Biology (GSB) Research Program
Women's Health Research Program
Research Programs Unit
HUS Gynecology and Obstetrics
Date: 2011
Language: eng
Number of pages: 5
Belongs to series: Orphanet journal of rare diseases
ISSN: 1750-1172
DOI: https://doi.org/10.1186/1750-1172-6-53
URI: http://hdl.handle.net/10138/162340
Subject: KUSTER-HAUSER-SYNDROME
LERI-WEILL DYSCHONDROSTEOSIS
IDIOPATHIC SHORT STATURE
CONTAINING GENE SHOX
X-CHROMOSOME
PRIMARY AMENORRHEA
TURNER SYNDROME
MRKH SYNDROME
DELETION
DOWNSTREAM
3123 Gynaecology and paediatrics
Peer reviewed: Yes
Rights: cc_by
Usage restriction: openAccess
Self-archived version: publishedVersion


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