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The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome.
Bamshad M, Le T, Watkins WS, Dixon ME, Kramer BE, Roeder AD, Carey JC, Root S, Schinzel A, Van Maldergem L, Gardner RJ, Lin RC, Seidman CE, Seidman JG, Wallerstein R, Moran E, Sutphen R, Campbell CE, Jorde LB. Bamshad M, et al. Among authors: jorde lb. Am J Hum Genet. 1999 Jun;64(6):1550-62. doi: 10.1086/302417. Am J Hum Genet. 1999. PMID: 10330342 Free PMC article.
A BglII RFLP near the human neurofibromatosis type 1 (NF1) gene.
Watkins WS, O'Connell P, Stevens J, Culver M, Ewart A, Jorde LB. Watkins WS, et al. Among authors: jorde lb. Nucleic Acids Res. 1991 Dec 11;19(23):6662. doi: 10.1093/nar/19.23.6662. Nucleic Acids Res. 1991. PMID: 1684425 Free PMC article.
Complex segregation analysis of autism.
Jorde LB, Hasstedt SJ, Ritvo ER, Mason-Brothers A, Freeman BJ, Pingree C, McMahon WM, Petersen B, Jenson WR, Mo A. Jorde LB, et al. Am J Hum Genet. 1991 Nov;49(5):932-8. Am J Hum Genet. 1991. PMID: 1928098 Free PMC article.
268 results