In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2 | Journal of Medical Genetics

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Cognitive and behavioural genetics

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In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2

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	Abstract	Full	Pdf
Nov 2022	1468	1041	121
Dec 2022	305	309	43
Jan 2023	243	241	46
Feb 2023	116	112	40
Mar 2023	106	92	25
Apr 2023	143	134	55
May 2023	483	481	75
Jun 2023	238	222	46
Jul 2023	304	286	41
Aug 2023	132	120	29
Sep 2023	105	97	34
Oct 2023	248	241	41
Nov 2023	451	447	32
Dec 2023	251	200	40
Jan 2024	96	80	241
Feb 2024	93	66	47
Mar 2024	103	95	49
Total	4885	4264	1005