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Volume 54, Issue 12
Expanding the clinical spectrum of recessive truncating mutations of KLHL7 to a Bohring-Opitz-like phenotype
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Developmental defects
Short report
Expanding the clinical spectrum of recessive truncating mutations of
KLHL7
to a Bohring-Opitz-like phenotype
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Online download statistics by month: October 2017 to February 2024
Abstract
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Oct 2017
323
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12
Nov 2017
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29
Dec 2017
331
42
25
Jan 2018
240
35
15
Feb 2018
170
12
7
Mar 2018
255
29
15
Apr 2018
157
29
14
May 2018
240
24
15
Jun 2018
188
17
17
Jul 2018
123
10
8
Aug 2018
84
11
5
Sep 2018
95
5
5
Oct 2018
77
7
9
Nov 2018
122
15
13
Dec 2018
81
7
3
Jan 2019
128
9
5
Feb 2019
71
9
5
Mar 2019
94
13
3
Apr 2019
53
17
8
May 2019
67
8
6
Jun 2019
62
13
9
Jul 2019
52
7
4
Aug 2019
77
8
5
Sep 2019
47
1
1
Oct 2019
64
8
2
Nov 2019
40
3
2
Dec 2019
95
5
1
Jan 2020
99
11
4
Feb 2020
44
2
1
Mar 2020
14
2
1
Apr 2020
44
12
6
May 2020
34
4
2
Jun 2020
77
8
6
Jul 2020
36
4
4
Aug 2020
33
5
5
Sep 2020
50
8
4
Oct 2020
65
6
5
Nov 2020
63
7
5
Dec 2020
62
11
12
Jan 2021
59
11
2
Feb 2021
90
6
7
Mar 2021
57
15
5
Apr 2021
38
6
5
May 2021
38
5
5
Jun 2021
8
4
7
Jul 2021
7
6
3
Aug 2021
3
3
1
Sep 2021
7
7
8
Oct 2021
55
12
8
Nov 2021
90
8
8
Dec 2021
71
6
6
Jan 2022
195
9
9
Feb 2022
79
7
5
Mar 2022
65
4
1
Apr 2022
43
11
6
May 2022
87
6
6
Jun 2022
71
6
5
Jul 2022
76
18
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Aug 2022
84
6
1
Sep 2022
106
13
7
Oct 2022
94
4
4
Nov 2022
60
6
2
Dec 2022
54
3
3
Jan 2023
59
5
2
Feb 2023
59
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1
Mar 2023
58
9
5
Apr 2023
42
2
1
May 2023
67
5
23
Jun 2023
29
8
6
Jul 2023
35
3
0
Aug 2023
47
4
2
Sep 2023
34
5
3
Oct 2023
28
0
1
Nov 2023
91
6
4
Dec 2023
91
2
2
Jan 2024
77
6
4
Feb 2024
152
4
4
Total
6903
759
479
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