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Human Molecular Genetics|March 21, 1998
Mutations of the alpha2(V) chain of type V collagen impair matrix assembly and produce ehlers-danlos syndrome type IK Michalickova, M Susic, M C Willing, et al.Human Molecular Genetics|November 1, 1996
A splice-junction mutation in the region of COL5A1 that codes for the carboxyl propeptide of pro alpha 1(V) chains results in the gravis form of the Ehlers-Danlos syndrome (type I)R J Wenstrup, G T Langland, M C Willing, et al.Genomics|September 16, 1999
Osteocalcin: genetic and physical mapping of the human gene BGLAP and its potential role in postmenopausal osteoporosisM H Raymond, B C Schutte, J C Torner, et al.The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|December 24, 1997
Determinants of bone mineral density in postmenopausal white IowansM C Willing, J C Torner, T L Burns, et al.The Journal of Biological Chemistry|June 15, 1988
Heterozygosity for a large deletion in the alpha 2(I) collagen gene has a dramatic effect on type I collagen secretion and produces perinatal lethal osteogenesis imperfectaM C Willing, D H Cohn, B Starman, et al.American Journal of Human Genetics|April 25, 2000
COL5A1 haploinsufficiency is a common molecular mechanism underlying the classical form of EDSR J Wenstrup, J B Florer, M C Willing, et al.Pediatrics|June 5, 2001
Physical activity and bone measures in young children: the Iowa bone development studyK F Janz, T L Burns, J C Torner, et al.Human Genetics|May 1, 1991
Osteogenesis imperfecta due to recurrent point mutations at CpG dinucleotides in the COL1A1 gene of type I collagenC J Pruchno, D H Cohn, G A Wallis, et al.American Journal of Human Genetics|October 1, 1994
Osteogenesis imperfecta type I: molecular heterogeneity for COL1A1 null alleles of type I collagenM C Willing, S P Deschenes, D A Scott, et al.Caries Research|April 18, 2012
Genetic and environmental factors associated with dental caries in children: the Iowa Fluoride StudyX Wang, M C Willing, M L Marazita, et al.Pageof 3