TBX6, LHX1 and copy number variations in the complex genetics of Mullerian aplasia

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http://hdl.handle.net/10138/162349

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Sandbacka , M , Laivuori , H , Freitas , E , Halttunen , M , Jokimaa , V , Morin-Papunen , L , Rosenberg , C & Aittomäki , K 2013 , ' TBX6, LHX1 and copy number variations in the complex genetics of Mullerian aplasia ' , Orphanet journal of rare diseases , vol. 8 , 125 . https://doi.org/10.1186/1750-1172-8-125

Title: TBX6, LHX1 and copy number variations in the complex genetics of Mullerian aplasia
Author: Sandbacka, Maria; Laivuori, Hannele; Freitas, Erika; Halttunen, Mervi; Jokimaa, Varpu; Morin-Papunen, Laure; Rosenberg, Carla; Aittomäki, Kristiina
Contributor: University of Helsinki, Haartman Institute (-2014)
University of Helsinki, Haartman Institute (-2014)
University of Helsinki, Clinicum
University of Helsinki, Department of Medical and Clinical Genetics
Date: 2013-08-16
Language: eng
Number of pages: 13
Belongs to series: Orphanet journal of rare diseases
ISSN: 1750-1172
URI: http://hdl.handle.net/10138/162349
Subject: KUSTER-HAUSER-SYNDROME
DOMINANT SPONDYLOCOSTAL DYSOSTOSIS
FEMALE REPRODUCTIVE-TRACT
192 CHINESE WOMEN
DUCT ABNORMALITIES
CONGENITAL ABSENCE
MOUSE EMBRYOS
MRKH SYNDROME
SEQUENCE VARIATIONS
PRIMARY AMENORRHEA
3111 Biomedicine
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