Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases | Journal of Medical Genetics

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Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases

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	Abstract	Full	Pdf
May 2022	1918	1856	266
Jun 2022	538	569	104
Jul 2022	345	331	61
Aug 2022	161	150	35
Sep 2022	132	120	43
Oct 2022	306	299	62
Nov 2022	176	168	62
Dec 2022	124	119	55
Jan 2023	109	110	57
Feb 2023	95	88	36
Mar 2023	109	89	51
Apr 2023	69	58	51
May 2023	103	91	50
Jun 2023	67	60	42
Jul 2023	57	50	20
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Sep 2023	70	64	18
Oct 2023	87	75	46
Nov 2023	77	51	30
Dec 2023	62	50	42
Jan 2024	37	31	23
Feb 2024	71	48	23
Mar 2024	63	71	142
Total	4840	4609	1344