Detalhe da pesquisa
1.
The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries.
Hum Mutat
; 40(11): e1-e23, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31209999
2.
Identification of 42 Genes Linked to Stage II Colorectal Cancer Metastatic Relapse.
Int J Mol Sci
; 17(5)2016 Apr 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-27136531
3.
Gender-associated genomic differences in colorectal cancer: clinical insight from feminization of male cancer cells.
Int J Mol Sci
; 15(10): 17344-65, 2014 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-25268611
4.
Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection.
Hum Mutat
; 32(1): 2-9, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21089065
5.
Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countries.
Fam Cancer
; 20(3): 215-221, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33098072
6.
Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project.
Genet Med
; 11(12): 843-9, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20010362
7.
Identification of a rare germline NBN gene mutation by whole exome sequencing in a lung-cancer survivor from a large family with various types of cancer.
Fam Cancer
; 16(3): 389-394, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27844240
8.
Next-generation sequencing in familial breast cancer patients from Lebanon.
BMC Med Genomics
; 10(1): 8, 2017 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28202063
9.
Wolcott-Rallison syndrome in a Bedouin boy.
Ann Saudi Med
; 24(6): 476-9, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15646169
10.
Impact of 226C>T MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing.
Fam Cancer
; 8(4): 289-98, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19669601