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Clinical Genetics|October 1, 1991
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian familiesA Turco, B Peissel, L Gammaro, et al.Prenatal Diagnosis|June 1, 1992
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reactionA Turco, B Peissel, P Quaia, et al.American Journal of Human Genetics|January 23, 1999
LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosisY Segal, B Peissel, A Renieri, et al.Clinical Genetics|October 15, 2013
The psychological impact of breast and ovarian cancer preventive options in BRCA1 and BRCA2 mutation carriersC Borreani, S Manoukian, E Bianchi, et al.Japanese Journal of Cancer Research : Gann|November 28, 2000
Mapping of melanoma modifier loci in RET transgenic miceT A Dragani, B Peissel, N Zanesi, et al.ESMO Open|July 10, 2022
Characterization of the HER2 status in BRCA-mutated breast cancer: a single institutional series and systematic review with pooled analysisG Tomasello, D Gambini, F Petrelli, et al.Nature Genetics|November 5, 1997
Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutationW Lu, B Peissel, H Babakhanlou, et al.Annals of Human Genetics|January 25, 2008
Reconstructing the genealogy of a BRCA1 founder mutation by phylogenetic analysisF Marroni, G Cipollini, B Peissel, et al.Journal of Perinatal Medicine|January 1, 1995
Gene linkage analysis and DNA based detection of autosomal dominant polycystic kidney disease (ADPKD) in a newborn infant. Case reportA E Turco, E M Padovani, B Peissel, et al.American Journal of Medical Genetics|December 1, 1993
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresiaA E Turco, B Peissel, S Rossetti, et al.Pageof 2