about
Comparative screening of FMF mutations in various communities of the Israeli society.CHANGES IN MARRIAGE PATTERNS AMONG THE ARAB COMMUNITY IN ISRAEL OVER A 60-YEAR PERIOD.Factors affecting the utilization of genetic counseling services among Israeli Arab women.Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy.A new case confirming and expanding the phenotype spectrum of ADAT3-related intellectual disability syndromeThe changing pattern of consanguinity in a selected region of the Israeli Arab communityExploration of Risk Factors for Type 2 Diabetes among Arabs in IsraelA novel biallelic loss-of-function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro-facio-thoracic dysplasia
P50
Q40250575-87FBBE60-823B-4682-A38C-45ECAFB5DC70Q40915240-EA3058D3-3059-483B-B474-6DB0C5CA93A3Q41685279-901D1283-1257-4E65-AF73-1C28CAA893CCQ53412801-8C90B8FF-46CE-448A-A647-3C7DD20370A0Q57184386-3FE15755-B4C6-48A6-8773-BA72A772626CQ81450307-FA0E9FD1-6679-46AE-8232-BEBE764005A8Q91912604-87CF85DB-E5BF-4DA1-A500-67D8D86FD9EBQ92129967-28397E4B-A8D5-49B8-A501-AF2400C2924B
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Abdelnaser Zalan
@en
Abdelnaser Zalan
@nl
type
label
Abdelnaser Zalan
@en
Abdelnaser Zalan
@nl
prefLabel
Abdelnaser Zalan
@en
Abdelnaser Zalan
@nl
P31
P496
0000-0003-4776-0675