J. Neidich

Racial disparity in maternal and fetal-cord bisphenol A concentrations

T. Hulsey, R. Newman, L. Guillette, 2012, Journal of Perinatology.

Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California.

Joshua L. Deignan, S. Cederbaum, J. Abdenur, 2012, Molecular genetics and metabolism.

Asymptomatic maternal combined homocystinuria and methylmalonic aciduria (cblC) detected through low carnitine levels on newborn screening.

Henry J. Lin, A. Jonas, D. Rosenblatt, 2009, The Journal of pediatrics.

The sensitivity and specificity of hyperglycosylated hCG (hhCG) levels to reliably diagnose clinical IVF pregnancies at 6 days following embryo transfer

C. Strom, R. Alvero, M. Cedars, 2012, Journal of Assisted Reproduction and Genetics.

Outcome of infants diagnosed with 3-methyl-crotonyl-CoA-carboxylase deficiency by newborn screening.

G. Enns, B. Graham, B. Lanpher, 2012, Molecular genetics and metabolism.

Maternal medium-chain acyl-CoA dehydrogenase deficiency identified by newborn screening.

J. Abdenur, J. Neidich, F. Lorey, 2011, Molecular genetics and metabolism.