A. M. Hack

Correlation of meiotic events in testis sections and microspreads of mouse spermatocytes relative to the mid-pachytene checkpoint

D. G. Rooij, L. Creemers, T. Ashley, 2004, Chromosoma.

Purification and properties of methylmalonyl coenzyme A mutase from human liver.

H. Willard, W. Fenton, L. Rosenberg, 1982, Archives of biochemistry and biophysics.

Stable Isotope Dilution Analysis of Isovalerylglycine in Amniotic Fluid and Urine and Its Application for the Prenatal Diagnosis of Isovaleric Acidemia

Kay Tanaka, S. Goodman, A. M. Hack, 1986, Pediatric Research.

DNA analysis for ornithine transcarbamylase deficiency

R. Rozen, A. Horwich, W. Fenton, 1986, Journal of Inherited Metabolic Disease.

Effect of the topoisomerase-II inhibitor etoposide on meiotic recombination in male mice.

P. Hunsicker, T. Ashley, L. B. Russell, 2000, Mutation research.

Prenatal diagnosis of ornithine transcarbamylase deficiency with use of DNA polymorphisms.

S. Brusilow, R. Rozen, W. Fenton, 1986, The New England journal of medicine.

Biogenesis of the mitochondrial enzyme methylmalonyl-CoA mutase. Synthesis and processing of a precursor in a cell-free system and in cultured cells.

W. Fenton, L. Rosenberg, A. M. Hack, 1984, The Journal of biological chemistry.

Identification and application of additional restriction fragment length polymorphisms at the human ornithine transcarbamylase locus.

W. Fenton, L. Rosenberg, A. M. Hack, 1986, American journal of human genetics.

Simple method for identification of plasmid-coded proteins

A. Sancar, A. M. Hack, W. Rupp, 1979, Journal of bacteriology.

Immunochemical studies of fibroblasts from patients with methylmalonyl-CoA mutase apoenzyme deficiency: detection of a mutation interfering with mitochondrial import.

W. Fenton, J. Kraus, L. Rosenberg, 1987, Proceedings of the National Academy of Sciences of the United States of America.