Novel NSDHL gene variant for congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome | BMJ Case Reports

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Case report

Novel NSDHL gene variant for congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome

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Online download statistics by month: November 2020 to April 2024

	Abstract	Full	Pdf
Nov 2020	489	16	13
Dec 2020	280	6	2
Jan 2021	123	3	1
Feb 2021	114	7	2
Mar 2021	82	2	2
Apr 2021	47	5	0
May 2021	17	1	1
Jun 2021	5	5	2
Jul 2021	4	1	0
Aug 2021	2	3	1
Sep 2021	3	3	1
Oct 2021	16	5	1
Nov 2021	57	3	1
Dec 2021	48	4	2
Jan 2022	23	4	0
Feb 2022	22	0	0
Mar 2022	60	17	0
Apr 2022	26	0	0
May 2022	40	0	0
Jun 2022	36	4	1
Jul 2022	14	2	0
Aug 2022	42	4	1
Sep 2022	74	2	3
Oct 2022	42	2	1
Nov 2022	37	2	2
Dec 2022	24	0	0
Jan 2023	31	0	0
Feb 2023	44	0	1
Mar 2023	24	0	1
Apr 2023	58	0	0
May 2023	25	2	2
Jun 2023	12	0	0
Jul 2023	52	0	0
Aug 2023	8	0	0
Sep 2023	15	1	0
Oct 2023	23	0	0
Nov 2023	16	1	0
Dec 2023	31	1	0
Jan 2024	32	1	0
Feb 2024	56	0	0
Mar 2024	28	3	1
Apr 2024	12	2	1
Total	2194	112	43