Case report of whole genome sequencing in the XY female: identification of a novel SRY mutation and revision of a misdiagnosis of androgen insensitivity syndrome
Crossref DOI link: https://doi.org/10.1186/s12902-016-0141-7
Published Online: 2016-11-08
Published Print: 2016-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
De Sousa, Sunita M. C.
Kassahn, Karin S.
McIntyre, Liam C.
Chong, Chan-Eng
Scott, Hamish S.
Torpy, David J.
Funding for this research was provided by:
National Health and Medical Research Council (APP1023059, APP1115188)
License valid from 2016-11-08