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Human Reproduction (Oxford, England)|February 1, 1986
Reproductive failure and parental chromosome abnormalitiesA Adamoli, F Bernardi, G Chiaffoni, et al.Human Genetics|January 1, 1981
Activity of steroid sulfatase in fibroblasts with numerical and structural X chromosome aberrationsH H Ropers, B Migl, J Zimmer, et al.Human Genetics|January 1, 1989
Localization of Y chromosome sequences and X chromosomal replication studies in XX malesW Schempp, G Müller, G Scherer, et al.Leukemia|January 17, 2009
The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndromeA Minelli, E Maserati, E Nicolis, et al.Human Genetics|January 1, 1984
Diagnostic application of first trimester trophoblast sampling in 100 pregnanciesG Simoni, B Brambati, C Danesino, et al.Cancer Genetics and Cytogenetics|October 1, 1993
Cytogenetics of multiple endocrine neoplasia syndromes. III. Analysis of an insulinoma from a subject with MEN 1 by chromosome paintingP Maraschio, A Pezzolo, M L Brandi, et al.Journal of Medical Genetics|October 1, 1992
Extravillus dividing fetal cells at CVS: evidence of their erythroblastic originG Terzoli, R Cartolano, F Rossella, et al.Human Genetics|April 17, 1979
Familial XX true hermaphroditism and the H-Y antigenM Fraccaro, L Tiepolo, O Zuffardi, et al.Human Genetics|January 1, 1983
Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancyG Simoni, B Brambati, C Danesino, et al.Human Genetics|January 1, 1982
High prevalence of Werner's syndrome in Sardinia. Description of six patients and estimate of the gene frequencyD Cerimele, F Cottoni, S Scappaticci, et al.Pageof 9