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Cancer Genetics and Cytogenetics|November 1, 1989
Clonal chromosome abnormalities with preferential involvement of chromosome 3 in patients with porokeratosis of MibelliS Scappaticci, S Lambiase, G Orecchia, et al.Annales De Genetique|September 1, 1977
X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromereP Maraschio, S Scappaticci, E Ferrari, et al.Humangenetik|January 1, 1975
A homozygote for a serum albumin variant of the slow typeC Petrini, F Giorcelli, F Porta, et al.Human Genetics|January 1, 1984
Y-dependent polypeptides identified by two-dimensional gel electrophoresis of monozygotic X0 and XY fibroblastsU Müller, N Maier, G Gimelli, et al.American Journal of Medical Genetics|May 1, 1989
A syndrome of primary gonadal failure, short stature, mitral valve prolapse, and mental retardationL Cantalamessa, M Baldini, B Ambrosi, et al.Human Genetics|September 19, 1978
The gene for human peptidase A is on band 18q23 and shows triplex and uniplex dosage effectC Danesino, A D'Azzo, P Maraschio, et al.The Journal of Clinical Endocrinology and Metabolism|April 1, 1997
Insulin-like growth factors (IGF-I and IGF-II) and IGF-binding protein-3 production by fibroblasts of patients with Turner's syndrome in cultureA Barreca, D Larizza, G Damonte, et al.Cancer Genetics and Cytogenetics|November 14, 1997
Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic lossL Seghezzi, C Dellavecchia, E Maserati, et al.Human Genetics|October 1, 1990
A ZFY-negative 46,XX true hermaphrodite is positive for the Y pseudoautosomal boundaryR J Jäger, C Ebensperger, M Fraccaro, et al.Clinical Genetics|September 1, 1986
The fetal pathology of the XXXXY-syndromeH Rehder, M Fraccaro, C Cuoco, et al.Pageof 9