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Canadian Family Physician Medecin De Famille Canadien|September 18, 2007
Papanicolaou smears: to swab or not to swabNarpinder Hans, Andrew J Cave, Olga Szafran, et al.
Clinical and Experimental Dermatology|May 9, 2008
Progressive symmetrical erythrokeratoderma: report of a Turkish family and evaluation for loricrin and connexin gene mutationsA Akman, M Masse, E Mihci, et al.
United European Gastroenterology Journal|March 12, 2016
Chronic constipation and co-morbidities: A prospective population-based nested case-control studyRok S Choung, Enrique Rey, G Richard Locke, et al.
Clinical and Experimental Dermatology|February 1, 2003
A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type KöbnerC M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
Pathologie-Biologie|May 1, 1992
[Bacteriostatic activity and killing curves of eight antibiotics against seven strains of penicillin G-resistant pneumococci]V Barakett, D Lesage, F Delisle, et al.
Gastroenterology|July 14, 2005
Prevalence and burden of fecal incontinence: a population-based study in womenAdil E Bharucha, Alan R Zinsmeister, G Richard Locke, et al.
The American Journal of Gastroenterology|February 9, 2006
Differences between painless and painful constipation among community womenAdil E Bharucha, G Richard Locke, Alan R Zinsmeister, et al.
The American Journal of Gastroenterology|June 15, 2006
Risk factors for fecal incontinence: a population-based study in womenAdil E Bharucha, Alan R Zinsmeister, G Richard Locke, et al.
Experimental Dermatology|February 13, 2001
Darier disease--novel mutations in ATP2A2 and genotype-phenotype correlationF Ringpfeil, A Raus, J J DiGiovanna, et al.
Human Genetics|December 18, 1998
Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratodermaG Richard, T W White, L E Smith, et al.
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