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Volume 17, Issue 2
46,XX disorder of sex development associated with skin abnormalities due to homozygous R-Spondin 1 loss of function mutation
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Case Reports: Rare disease
46,XX disorder of sex development associated with skin abnormalities due to homozygous R-Spondin 1 loss of function mutation
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Online download statistics by month: February 2024 to October 2024
Abstract
Full
Pdf
Feb 2024
531
21
15
Mar 2024
245
6
5
Apr 2024
139
3
1
May 2024
144
3
1
Jun 2024
88
9
5
Jul 2024
46
2
1
Aug 2024
72
2
3
Sep 2024
57
0
0
Oct 2024
61
2
1
Total
1383
48
32
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