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Current Opinion in Neurology|April 1, 1994
Advances in understanding the development of the nervous systemH S Singer, A Y Chiu, K F Meiri, et al.
American Journal of Human Genetics|September 1, 1996
Family study and segregation analysis of Tourette syndrome: evidence for a mixed model of inheritanceJ T Walkup, M C LaBuda, H S Singer, et al.
Pediatrics|August 1, 1996
The risk of seizure recurrence after a first unprovoked afebrile seizure in childhood: an extended follow-upS Shinnar, A T Berg, S L Moshe, et al.
The Journal of Pediatrics|November 1, 1982
Carnitine deficiency presenting as familial cardiomyopathy: a treatable defect in carnitine transportL J Waber, D Valle, C Neill, et al.
Human Molecular Genetics|November 1, 1993
Expression and processing of human ornithine-delta-aminotransferase in Saccharomyces cerevisiaeK M Dougherty, D A Swanson, L C Brody, et al.
Genomics|August 1, 1993
Isolation and characterization of an ornithine aminotransferase-related sequence (OATL3) mapping to 10q26M T Geraghty, W G Kearns, P L Pearson, et al.
Genomics|November 1, 1989
A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndromeT Glaser, D J Driscoll, S Antonarakis, et al.
The New England Journal of Medicine|June 7, 1990
Allopurinol-induced orotidinuria. A test for mutations at the ornithine carbamoyltransferase locus in womenE R Hauser, J E Finkelstein, D Valle, et al.
American Journal of Medical Genetics|February 15, 2001
Cervical stenosis secondary to rhizomelic chondrodysplasia punctataA J Khanna, N E Braverman, D Valle, et al.
Human Genetics|May 1, 1992
Phenotype of disease in three patients with identical mutations in methylmalonyl CoA mutaseA M Crane, L S Martin, D Valle, et al.
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