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American Journal of Human Genetics|August 1, 1992
Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35K D Mathews, K A Mills, E P Bosch, et al.Journal of Medical Genetics|August 6, 2002
Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial cleftsL L Barrow, H van Bokhoven, S Daack-Hirsch, et al.American Journal of Human Genetics|March 1, 1996
Orofacial clefts, parental cigarette smoking, and transforming growth factor-alpha gene variantsG M Shaw, C R Wasserman, E J Lammer, et al.Genomics|January 1, 1989
Mapping of the human complement factor I gene to 4q25R Shiang, J C Murray, C C Morton, et al.Journal of Perinatology : Official Journal of the California Perinatal Association|September 15, 2007
Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm deliveryK M Steffen, M E Cooper, M Shi, et al.Allergy|August 13, 2003
Breastfeeding and allergic disease: a multidisciplinary review of the literature (1966-2001) on the mode of early feeding in infancy and its impact on later atopic manifestationsJ van Odijk, I Kull, M P Borres, et al.Genomics|February 1, 1988
Regional assignment of the gene for human liver/bone/kidney alkaline phosphatase to chromosome 1p36.1-p34M Smith, M J Weiss, C A Griffin, et al.Journal of Dental Research|August 3, 2017
Disrupted IRF6-NME1/2 Complexes as a Cause of Cleft Lip/PalateM T Parada-Sanchez, E Y Chu, L L Cox, et al.Nature Genetics|April 1, 1994
Integrated human genome-wide maps constructed using the CEPH reference panelK H Buetow, J L Weber, S Ludwigsen, et al.Diabetes|August 1, 1989
Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13G I Bell, J C Murray, Y Nakamura, et al.Pageof 32