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Human Mutation|August 31, 2002
SNP databases and pharmacogenetics: great start, but a long way to goSharon Marsh, Pui Kwok, Howard L McLeodHuman Mutation|August 31, 2002
Mutational analysis of patients with the diagnosis of choroideremiaKerry E McTaggart, Mai Tran, Dean Y Mah, et al.Human Mutation|August 31, 2002
Population genetic implications from DNA polymorphism in random human genomic sequencesPeidong Shen, Molly Buchholz, Raphael Sung, et al.Human Mutation|August 31, 2002
Rapid detection of novel BRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragmentsFederica Casilli, Zorika Christiana Di Rocco, Sophie Gad, et al.Human Mutation|August 31, 2002
Third international meeting on the genetic epidemiology of complex traits, April 4-6, 2002, Cambridge, UKSally John, Suzanne JenkinsHuman Mutation|August 31, 2002
Large Family With Maturity-Onset Diabetes of the Young and a Novel V121I Mutation in HNF4ACarole T Monney, Valérie Kaltenrieder, Pascal Cousin, et al.Human Mutation|August 31, 2002
Identification of seven novel mutations of F8C by DHPLCSabrina Frusconi, Ilaria Passerini, Francesca Girolami, et al.Human Mutation|January 17, 2002
Mutations and polymorphisms in the human ornithine transcarbamylase geneMendel Tuchman, Naser Jaleel, Hiroki Morizono, et al.Human Mutation|January 17, 2002
Polymorphisms and HNPCC: PMS2-MLH1 protein interactions diminished by single nucleotide polymorphismsZi Qiang Yuan, Bruce Gottlieb, Lenore K Beitel, et al.Human Mutation|January 17, 2002
Identification of seven novel missense mutations, two splice-site mutations, two microdeletions and a polymorphic amino acid substitution in the gene for ornithine transcarbamylase (OTC) in patients with OTC deficiencyConsuelo Climent, Vicente RubioPageof 574