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Blood|May 1, 1983
Red blood cell glucose metabolism in trisomy 10p: possible role of hexokinase in the erythrocyteM Magnani, V Stocchi, E Piatti, et al.
Prenatal Diagnosis|October 1, 1983
Prenatal prediction of duplication 10q24 leads to qter by gene dosage of GOT1 on uncultured amniotic cellsB Dallapiccola, G Novelli, G Micara, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|May 1, 1990
[Specific enzymatic amplification of a DNA region closely associated with Huntington chorea]G Novelli, P Mandich, A Ruzzo, et al.
Annales De Genetique|January 1, 1996
Myoclonic epilepsy, neuroblast migration disorders, and maternally derived partial duplication 14q/deletion 15qP Iannetti, A Spalice, R Mingarelli, et al.
Human Genetics|January 1, 1981
Acute lymphocytic and myelomonocytic leukemia associated with low platelet counts and a 21q- marker chromosomeG Alimena, B Dallapiccola, M R De Cuia, et al.
American Journal of Medical Genetics|June 1, 1987
Common fragile sites: their prevalence in subjects with constitutional and acquired chromosomal instabilityB Tedeschi, B Porfirio, P Vernole, et al.
Acta Radiologica (Stockholm, Sweden : 1987)|January 1, 1994
Sister chromatid exchanges in cultured amniocytes exposed to diagnostic ultrasound in vitroB Porfirio, B Dallapiccola, C Cittanti, et al.
Human Genetics|September 22, 1977
Deletion of the long arm of chromosome 8 resulting from a de novo translocation t(4;8) (q13;q213)B Dallapiccola, L Santoro, S Trabace, et al.
Prenatal Diagnosis|April 1, 1994
Prenatal diagnosis of X-linked retinitis pigmentosa (RP) in five pregnancies at riskM P Iampieri, R Mingarelli, E Le Guern, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 10, 2001
Targeted correction of a defective selectable marker gene in human epithelial cells by small DNA fragmentsA Colosimo, K K Goncz, G Novelli, et al.
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