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Human Genetics|June 1, 1993
Two new polymorphisms in the coding sequence of the LDL receptor (LDLR) geneB Saint-Jore, N Loux, C Junien, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|August 11, 2001
Molecular analysis of apo(a) fragmentation in polygenic hypercholesterolemia: characterization of a new plasma fragment patternS Gonbert, B Saint-Jore, P Giral, et al.Genomics|October 29, 1998
Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11B Funke, A Puech, B Saint-Jore, et al.Human Molecular Genetics|November 13, 1998
Goosecoid-like (Gscl), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse developmentB Saint-Jore, A Puech, J Heyer, et al.Human Mutation|January 1, 1997
Familial ligand-defective apolipoprotein B-100: simultaneous detection of the ARG3500-->GLN and ARG3531-->CYS mutations in a French populationJ P Rabès, M Varret, B Saint-Jore, et al.Genomics|June 1, 1997
Identification, characterization, and precise mapping of a human gene encoding a novel membrane-spanning protein from the 22q11 region deleted in velo-cardio-facial syndromeH Sirotkin, B Morrow, B Saint-Jore, et al.Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome regionA Puech, B Saint-Jore, S Merscher, et al.Human Mutation|January 1, 1992
Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism methodN Loux, B Saint-Jore, G Collod, et al.Genomics|January 27, 1998
Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11B Funke, B Saint-Jore, A Puech, et al.Proceedings of the National Academy of Sciences of the United States of America|February 7, 1998
Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organizationA Puech, B Saint-Jore, B Funke, et al.Pageof 2