statistiche ricercatore

Nome	#
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder	142
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder	119
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome	118
Unique genomic profile associated with pediatric uveal melanoma	113
Variable expressivity of a familial 1.9 Mb microdeletion in 3q28 leading to haploinsufficiency of TP63: Refinement of the critical region for a new microdeletion phenotype	108
Variable expressivity of a familial 1.9 Mb microdeletion in 3q28 leading to haploinsufficiency of TP63: Refinement of the critical region for a new microdeletion phenotype.	78
Variable expressivity of a familial 1.9 Mb microdeletion in 3q28 leading to haploinsufficiency of TP63: Refinement of the critical region for a new microdeletion phenotype.	57
Totale	735

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	115	15	20	11	4	2	11	13	7	4	5	14	9
2020/2021	68	2	10	1	8	11	2	3	3	10	2	16	0
2021/2022	73	3	5	0	6	4	5	0	16	4	4	12	14
2022/2023	188	30	26	15	30	8	27	9	16	15	2	6	4
2023/2024	78	3	14	1	9	2	21	3	0	0	2	11	12
2024/2025	4	4	0	0	0	0	0	0	0	0	0	0	0
Totale													735

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