statistiche ricercatore

Nome	#
Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblings	71
SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss	48
Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss	32
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss	31
R75Q dominant mutation in GJB2 gene silenced by the in Cis recessive mutation c.35delG	27
Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme	27
Totale	236

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	28	9	0	0	1	2	1	2	4	0	0	3	6
2020/2021	33	3	2	3	4	3	3	4	5	2	1	1	2
2021/2022	43	2	1	2	4	0	0	2	1	8	4	7	12
2022/2023	71	6	5	5	2	13	7	2	7	10	9	2	3
2023/2024	34	3	8	0	5	3	7	1	7	0	0	0	0
Totale													236