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Recurrent microdeletion at 17q12 as a cause of Mayer-Rokita..:
Bernardini, Laura
;
Gimelli, Stefania
;
Gervasini, Cristina
...
Orphanet Journal of Rare Diseases. 4 (2009) 1 - p. , 2009
Link:
https://doi.org/10.1186/1750-1172-4-25
RT Journal T1
Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_1750-1172-4-25&Exemplar=1&LAN=DE A1 Bernardini, Laura A1 Gimelli, Stefania A1 Gervasini, Cristina A1 Carella, Massimo A1 Baban, Anwar A1 Frontino, Giada A1 Barbano, Giancarlo A1 Divizia, Maria Teresa A1 Fedele, Luigi A1 Novelli, Antonio A1 Béna, Frédérique A1 Lalatta, Faustina A1 Miozzo, Monica A1 Dallapiccola, Bruno PB Springer Science and Business Media LLC YR 2009 SN 1750-1172 JF Orphanet Journal of Rare Diseases VO 4 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/1750-1172-4-25 DO https://doi.org/10.1186/1750-1172-4-25 SF ELIB - SuUB Bremen
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