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Allelic spectrum of formiminotransferase-cyclodeaminase gene variants in individuals with formiminoglutamic aciduria.
Mol Genet Genomic Med. 2017 Nov;5(6):795-799. doi: 10.1002/mgg3.333. Epub 2017 Sep 11.
Mol Genet Genomic Med. 2017.
PMID: 29178637
Free PMC article.
Characteristics and outcomes of patients with formiminoglutamic aciduria detected through newborn screening.
Ahrens-Nicklas RC, Ganetzky RD, Rush PW, Conway RL, Ficicioglu C.
Ahrens-Nicklas RC, et al. Among authors: rush pw.
J Inherit Metab Dis. 2019 Jan;42(1):140-146. doi: 10.1002/jimd.12035.
J Inherit Metab Dis. 2019.
PMID: 30740726
Free PMC article.
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Fetal echogenic bowel and a dilated loop of bowel associated with cystic fibrosis (CF) mutations delta F508 and 2183AA-->G.
Rush PW, Vats S, Allitto BA, Qureshi F, Feldman GL.
Rush PW, et al.
Prenat Diagn. 1998 Jun;18(6):638-40.
Prenat Diagn. 1998.
PMID: 9664617
No abstract available.
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Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect.
Manji S, Roberson JR, Wiktor A, Vats S, Rush P, Diment S, Van Dyke DL.
Manji S, et al.
Genet Med. 2001 Jan-Feb;3(1):65-6. doi: 10.1097/00125817-200101000-00014.
Genet Med. 2001.
PMID: 11339382
Free article.
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