Search details
1.
Deep dermatophytosis and inherited CARD9 deficiency.
N Engl J Med
; 369(18): 1704-1714, 2013 Oct 31.
Article
in English
| MEDLINE | ID: mdl-24131138
2.
From -omics to personalized medicine in nephrology: integration is the key.
Nephrol Dial Transplant
; 28(1): 24-8, 2013 Jan.
Article
in English
| MEDLINE | ID: mdl-23229923
3.
Prevalence of genetic variants associated with inflammatory bowel disease in a healthy First Nations cohort.
CMAJ
; 184(8): E435-41, 2012 May 15.
Article
in English
| MEDLINE | ID: mdl-22496383
4.
Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription.
Cell Metab
; 31(6): 1107-1119.e12, 2020 06 02.
Article
in English
| MEDLINE | ID: mdl-32492392
5.
Two-stage candidate gene study of chromosome 3p demonstrates an association between nonsynonymous variants in the MST1R gene and Crohn's disease.
Inflamm Bowel Dis
; 14(4): 500-7, 2008 Apr.
Article
in English
| MEDLINE | ID: mdl-18200509
6.
Contribution of the novel inflammatory bowel disease gene IL23R to disease susceptibility and phenotype.
Inflamm Bowel Dis
; 13(9): 1063-8, 2007 Sep.
Article
in English
| MEDLINE | ID: mdl-17508420
7.
Confirmation of the role of ATG16L1 as a Crohn's disease susceptibility gene.
Inflamm Bowel Dis
; 13(8): 941-6, 2007 Aug.
Article
in English
| MEDLINE | ID: mdl-17455206
8.
Association between genetic variants in myosin IXB and Crohn's disease.
Inflamm Bowel Dis
; 15(7): 1014-21, 2009 Jul.
Article
in English
| MEDLINE | ID: mdl-19235913
9.
Clinical and molecular characteristics of isolated colonic Crohn's disease.
Inflamm Bowel Dis
; 14(12): 1667-77, 2008 Dec.
Article
in English
| MEDLINE | ID: mdl-18521924
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