French Canadian
Identification of a novel truncating PALB2mutation and analysis of its contribution to early onset breast cancer in French Canadian women
9
BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high risk French Canadian families
12
Quality of life in multiple sclerosis: translation in French Canadian of the MSQoL-54
7
Common low density lipoprotein receptor mutations in the French Canadian population
11
Hereditary C7 deficiency Diagnosis and HLA studies in a French Canadian family
10
Screening of novel restless legs syndrome–associated genes in French-Canadian families
6
Development and relative validation of a food frequency questionnaire for French-Canadian adolescent and young adult survivors of acute lymphoblastic leukemia
12
Representations of language education in English and French Canadian newspapers
37
Validation of the French Canadian version of the Expanded Prostate Cancer Index Composite (EPIC) in a French Canadian population
15
Validity and reproducibility of an interviewer-administered food frequency questionnaire for healthy French-Canadian men and women
10
Type 1 hereditary tyrosinemia Evidence for molecular heterogeneity and identification of a causal mutation in a French Canadian patient
9
Familial Hypercholesterolemia: Molecular, Biochemical, and Clinical Characterization of a French-Canadian Pediatric Population
10
Validation of the French Canadian version of the Expanded Prostate Cancer Index Composite (EPIC) in a French Canadian population
7
A phonological and sociolinguistic survey of students in a French Canadian high school
128
Canadian French translation and linguistic validation of the child health utility 9D (CHU9D)
7
A targeted analysis identifies a high frequency of BRCA1 and BRCA2 mutation carriers in women with ovarian cancer from a founder population
10
N gram and Neural Language Models for Discriminating Similar Languages
8
Dental age estimation in southern Chinese population using panoramic radiographs: validation of three population specific reference datasets
8
FokI and BsmI Polymorphisms of the VDR Gene and Breast Cancer Risk
5
Multiple crm mutations in familial hypercholesterolemia Evidence for 13 alleles, including four deletions
10