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Phenotypical characterization of 13q deletion syndrome: Report of two cases

Eiman Bagherizadeh1, Yousef Shafaghati1, Fatemeh Hadipour1

  • 1Department of Medical Genetics, Sarem Cell Research Center, Sarem Hospital, Tehran, Iran.

Indian Journal of Human Genetics
|November 18, 2014
PubMed

Keywords:
13q deletion syndromemental retardationmultiple anomalies

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