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Peggy W. Rush

Observed name: Peggy Rush
OpenAlex ID: A5045900164
Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect
2001 · Shelina Manji, Jacquelyn R Roberson, et al. · Genetics in Medicine · 25
Allelic spectrum of formiminotransferase‐cyclodeaminase gene variants in individuals with formiminoglutamic aciduria
2017 · Ramanath Majumdar, Andrew Yori, et al. · Molecular Genetics & Genomic Medicine · 17
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Characteristics and outcomes of patients with formiminoglutamic aciduria detected through newborn screening
2019 · Rebecca C. Ahrens‐Nicklas, Rebecca D. Ganetzky, et al. · Journal of Inherited Metabolic Disease · 12
Fetal echogenic bowel and a dilated loop of bowel associated with cystic fibrosis (CF mutations ΔF508 and 2183AA→G
1998 · Peggy W. Rush, Subodh Vats, et al. · Prenatal Diagnosis · 4
Survival of Lethal Neonatal Cpt-ii Deficiency With High Dose Triheptanoin Therapy
2022 · Daniel J. Pomerantz, Peggy Rush, et al. · Molecular Genetics and Metabolism
Characteristics and outcomes of patients with formiminoglutamic aciduria detected through newborn screening
2018 · Rebecca C. Ahrens-Nicklas, Rebecca D. Ganetzky, et al. · Journal of Inherited Metabolic Disease
Works count: 6
Citation count: 58
H-index: 4
I10-index: 3
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