Open AccessTurner syndrome due to Xp22.33 deletion with preserved gonadal function: case report
Author(s) -
Fabiola D’Ambrosio,
Jacqueline Chan,
Hunain Aslam,
Roxana Aguirre Castañeda,
Lenika De Simone,
Zohra Shad
Publication year - 2019
Publication title -
oxford medical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.169
H-Index - 9
ISSN - 2053-8855
DOI - 10.1093/omcr/omz028
Subject(s) - karyotype , short stature , x chromosome , turner syndrome , genetics , menarche , y chromosome , medicine , biology , pediatrics , chromosome , gynecology , gene
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