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BMJ Journals
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Volume 57, Issue 7
De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities
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Novel disease loci
Short report
De novo variants in
SUPT16H
cause neurodevelopmental disorders associated with corpus callosum abnormalities
Online download statistics by month:
Online download statistics by month: January 2020 to October 2024
Abstract
Full
Pdf
Jan 2020
632
68
50
Feb 2020
243
27
15
Mar 2020
182
20
10
Apr 2020
65
8
4
May 2020
73
10
8
Jun 2020
377
37
18
Jul 2020
230
30
17
Aug 2020
114
13
9
Sep 2020
123
18
9
Oct 2020
95
13
5
Nov 2020
71
8
5
Dec 2020
101
19
6
Jan 2021
130
22
9
Feb 2021
132
20
14
Mar 2021
101
8
5
Apr 2021
160
8
4
May 2021
66
8
8
Jun 2021
11
11
5
Jul 2021
8
7
5
Aug 2021
14
13
8
Sep 2021
10
7
5
Oct 2021
76
12
7
Nov 2021
76
7
1
Dec 2021
107
18
7
Jan 2022
94
17
11
Feb 2022
70
10
3
Mar 2022
159
18
19
Apr 2022
195
18
12
May 2022
200
22
14
Jun 2022
125
15
7
Jul 2022
142
26
10
Aug 2022
111
11
8
Sep 2022
121
15
5
Oct 2022
120
9
3
Nov 2022
56
15
6
Dec 2022
62
5
2
Jan 2023
105
16
4
Feb 2023
75
6
5
Mar 2023
58
17
10
Apr 2023
118
3
2
May 2023
102
10
2
Jun 2023
43
1
2
Jul 2023
90
12
2
Aug 2023
113
11
4
Sep 2023
56
13
7
Oct 2023
56
6
4
Nov 2023
97
10
8
Dec 2023
78
13
7
Jan 2024
65
8
8
Feb 2024
76
5
12
Mar 2024
120
18
11
Apr 2024
69
16
11
May 2024
80
3
4
Jun 2024
73
3
3
Jul 2024
159
8
4
Aug 2024
101
10
3
Sep 2024
86
18
7
Oct 2024
92
4
4
Total
6564
804
458
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