Elizabeth McPherson
Medical Genetics
Marshfield Clinic
Marshfield
USA
Name/email consistency: high
- Extreme Values of Maternal Serum Analytes in Second Trimester Screening: Looking Beyond Trisomy and NTD's. McPherson, E., Thomas, G.D., Manlick, C., Zaleski, C.A., Reynolds, K.K., Rasmussen, K., Giampietro, P.F., Wiley, C., Mascola, M. J. Genet. Couns (2011)
- Ovarian failure and dilated cardiomyopathy due to a novel lamin mutation. McPherson, E., Turner, L., Zador, I., Reynolds, K., Macgregor, D., Giampietro, P.F. Am. J. Med. Genet. A (2009)
- Clinical genetics provider real-time workflow study. McPherson, E., Zaleski, C., Benishek, K., McCarty, C.A., Giampietro, P.F., Reynolds, K., Rasmussen, K. Genet. Med. (2008)
- Renal anomalies in families of individuals with congenital solitary kidney. McPherson, E. Genet. Med. (2007)
- Mitochondrial mutation in a child with distal arthrogryposis. McPherson, E., Zabel, C. Am. J. Med. Genet. A (2006)
- Genetic diagnosis and testing in clinical practice. McPherson, E. Clin. Med. Res (2006)
- Prenatal diagnosis of episodic tachypnea in an infant with OFD VI. McPherson, E., Zaleski, C., Mascola, M. Am. J. Med. Genet. A (2006)
- Tetrasomy 9q in an infant with cleft palate and multiple anomalies. McPherson, E., Neiswanger, K., Surti, U. Clin. Dysmorphol. (2005)
- Anomalies of the forebrain with radial limb defects: Garcia-Lurie-Steinfeld syndrome?. McPherson, E., Huff, D., Dunn, J., Muenke, M. Birth Defects Res. Part A Clin. Mol. Teratol. (2004)