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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.Human Genetics|January 19, 1979
A homozygote for a serum albumin variant of the fast typeG Vanzetti, F Porta, L Prencipe, et al.Mutation Research|May 1, 1989
Chromosome instability in lymphocytes from a patient with Werner's syndrome is not associated with DNA repair defectsM Stefanini, S Scappaticci, P Lagomarsini, et al.Clinical Endocrinology|November 28, 1997
Does growth hormone treatment increase chromosomal abnormalities?M Bozzola, K Tettoni, F Severi, et al.Human Genetics|June 10, 1977
Risk for recombinants in pericentric inversions of the (p11 leads to q21) region of chromosome 18V Vigi, P Maraschio, G Bosi, et al.Prenatal Diagnosis|January 1, 1983
Prenatal diagnosis, fetal pathology and cytogenetic analysis of a 46,XX/47,XX, + 15 mosaicG Gimelli, C Cuoco, E Porro, et al.Journal of Medical Genetics|August 1, 1977
15/15 translocation in Prader-Willi syndromeM Fraccaro, O Zuffardi, E M Buhler, et al.Cytogenetics and Cell Genetics|January 1, 1989
Analysis of complex Y chromosome aberrations using a single DNA probe (Y-367)U Müller, D Fontaine, M Adinolfi, et al.Human Genetics|May 1, 1992
Evidence for an ancestral alphoid domain on the long arm of human chromosome 2R Avarello, A Pedicini, A Caiulo, et al.Pageof 10