Susi Scappaticci

The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families

Lennart Iselius, J. Lindsten, Alain Aurias et al. · Human Genetics · 1983 · 189 citations

Human Migration, New Cases, Collaborative Study

Women heterozygous for deficiency of the (p21 ? pter) region of the X chromosome are fertile

M. Fraccaro, P Maraschio, Francesco Pasquali et al. · Human Genetics · 1977 · 87 citations

Infertility, Mendelian Disorder, Fertility +13

Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's syndrome

Susi Scappaticci, D. Cerimele, M. Fraccaro · Human Genetics · 1982 · 87 citations

Chromatin, Chromosome Dynamics, Developmental Biology +11

Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies

Carla Olivieri, Fabio Pagella, L Semino et al. · Journal of Human Genetics · 2007 · 65 citations · Full text

Allelic Variant, Hht Italian Families, Mendelian Disorder +11

Homozygosity Mapping of the Werner Syndrome Locus (WRN)

Jun Nakura, Ellen M. Wijsman, Tetsuro Miki et al. · Genomics · 1994 · 64 citations

Werner Syndrome Locus, Genetic Disorder, Genetics +4