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Genome Research|January 25, 2000
A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41B C Schutte, B C Bjork, K B Coppage, et al.
Critical Reviews in Food Science and Nutrition|March 18, 2014
Pregnancy and Infants' Outcome: Nutritional and Metabolic ImplicationsC Berti, I Cetin, C Agostoni, et al.
American Journal of Human Genetics|August 1, 1992
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qterC Wijmenga, L A Sandkuijl, P Moerer, et al.
American Journal of Human Genetics|March 1, 1990
Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome IqJ C Murray, D Y Nishimura, K H Buetow, et al.
Human Molecular Genetics|May 1, 1994
Localization of the achondroplasia gene to the distal 2.5 Mb of human chromosome 4pC A Francomano, R I Ortiz de Luna, T W Hefferon, et al.
Clinical Genetics|July 30, 2013
Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypesE Weh, L M Reis, R C Tyler, et al.
Gene Expression|January 5, 2002
Antagonistic regulation of Dlx2 expression by PITX2 and Msx2: implications for tooth developmentP D Green, T A Hjalt, D E Kirk, et al.
Arthritis and Rheumatism|February 1, 1995
Changes in cartilage composition and physical properties due to stromelysin degradationL J Bonassar, E H Frank, J C Murray, et al.
Scandinavian Journal of Public Health|January 5, 2002
The Danish National Birth Cohort--its background, structure and aimJ Olsen, M Melbye, S F Olsen, et al.
Ebiomedicine|August 8, 2018
Plasma Concentrations of Long Chain N-3 Fatty Acids in Early and Mid-Pregnancy and Risk of Early Preterm BirthS F Olsen, T I Halldorsson, A L Thorne-Lyman, et al.
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