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Human Molecular Genetics|April 1, 1996
Phenotypic variation in Waardenburg syndrome: mutational heterogeneity, modifier genes or polygenic background?A Pandya, X J Xia, B L Landa, et al.
Journal of Periodontology|December 29, 2000
Evidence of a substantial genetic basis for risk of adult periodontitisB S Michalowicz, S R Diehl, J C Gunsolley, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 5, 1997
Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992-1996T H Beaty, N E Maestri, J B Hetmanski, et al.
Oral Oncology|December 20, 2000
Smoking and alcohol in the etiology of oral cancer: gender-specific risk profiles in the south of GreeceA I Zavras, C W Douglass, K Joshipura, et al.
American Journal of Human Genetics|October 1, 1994
Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypesL A Farrer, K S Arnos, J H Asher, et al.
Genomics|December 1, 1987
Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17S R Diehl, M Boehnke, R P Erickson, et al.
American Journal of Human Genetics|February 1, 1996
Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndromeJ E Reynolds, M L Marazita, J M Meyer, et al.
American Journal of Human Genetics|January 1, 1989
A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) geneS R Diehl, M Boehnke, R P Erickson, et al.
British Journal of Cancer|November 19, 2011
Correlates of anti-EBV EBNA1 IgA positivity among unaffected relatives from nasopharyngeal carcinoma multiplex familiesC M Chang, K J Yu, W L Hsu, et al.
Journal of Craniofacial Genetics and Developmental Biology|December 10, 1999
Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutationS Beiraghi, A Miller-Chisholm, W J Kimberling, et al.
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