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Rare disease
CASE REPORT
Female phenotype with male karyotype: a clinical enigma

 

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Jun 201712835
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Aug 20174913
Sep 20177141
Oct 20176400
Nov 20179835
Dec 20172922
Jan 20181000
Feb 201818500
Mar 201816413
Apr 20183322
May 20186001
Jun 20183301
Jul 20182820
Aug 20184912
Sep 20183311
Oct 20184200
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Dec 2018114414
Jan 2019129621
Feb 2019304319
Mar 2019287117
Apr 2019205219
May 2019408014
Jun 2019310016
Jul 2019270013
Aug 2019230122
Sep 2019223011
Oct 2019321040
Nov 2019273026
Dec 201922305
Jan 2020226136
Feb 2020389295
Mar 2020406199
Apr 2020353031
May 2020375068
Jun 20205593132
Jul 2020447084
Aug 2020295132
Sep 20206192114
Oct 20205480105
Nov 2020277052
Dec 2020295156
Jan 2021302248
Feb 2021262045
Mar 2021455084
Apr 2021222057
May 202189059
Jun 20213138
Jul 20219330
Aug 2021206
Sep 2021411
Oct 20214723
Nov 20212902
Dec 20218216
Jan 20225308
Feb 20224027
Mar 20223903
Apr 20224804
May 20223822
Jun 20223601
Jul 20225113
Aug 20226714
Sep 20225642
Oct 20224003
Nov 20224113
Dec 20221921
Jan 20232600
Feb 20239432
Mar 20232443
Apr 20233832
May 20234110
Jun 20234901
Jul 20234202
Aug 20231610
Sep 20231711
Oct 20235000
Nov 20233603
Dec 20231410
Jan 20241910
Feb 20241510
Mar 20242011
Total121931021629