Skip to Main Content (Press Enter)

Logo UNIMI
  • ×
  • Home
  • People
  • Projects
  • Fields
  • Units
  • Outputs
  • Third Mission

Expertise & Skills
Logo UNIMI

|

Expertise & Skills

unimi.it
  • ×
  • Home
  • People
  • Projects
  • Fields
  • Units
  • Outputs
  • Third Mission
  1. Outputs

Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) sindrome: two case reports

Other Research Product
Publication Date:
2009
Citation:
Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) sindrome: two case reports / L. Bernardini, S. Gimelli, C. Gervasini, M. Carella, A. Baban, G. Frontino, G. Barbano, L. Fedele, A. Novelli, F. Lalatta, B. Dallapiccola. ((Intervento presentato al convegno European Conference of Human Genetics tenutosi a Vienna nel 2009.
IRIS type:
14 - Intervento a convegno non pubblicato
List of contributors:
L. Bernardini, S. Gimelli, C. Gervasini, M. Carella, A. Baban, G. Frontino, G. Barbano, L. Fedele, A. Novelli, F. Lalatta, B. Dallapiccola
Authors of the University:
GERVASINI CRISTINA COSTANZA GIOVANNA ( author )
Link to information sheet:
https://air.unimi.it/handle/2434/72258
  • Research Areas

Research Areas

Concepts


Settore MED/03 - Genetica Medica
  • Guide
  • Help
  • Accessibility
  • Privacy
  • Use of cookies
  • Legal notices

Powered by VIVO | Designed by Cineca | 26.7.0.0