Detalhe da pesquisa
1.
Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities.
Cold Spring Harb Mol Case Stud
; 6(5)2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33028645
2.
Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families.
Eur J Hum Genet
; 24(10): 1430-5, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27049303
3.
Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.
Eur J Hum Genet
; 18(4): 407-13, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19888295