V. Markovic

发表

Methylation of the 5′ flanking sequences of the ribosomal DNA in human cell lines and in a human‐hamster hybird cell line

M. Rocchi, D. Miller, A. Baldini, 1992, Journal of cellular biochemistry.

Age-associated chromosome 21 loss in Down syndrome: possible relevance to mosaicism and Alzheimer disease.

M. Somerville, A. Dalton, M. Percy, 1993, American journal of medical genetics.

Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome

M. W. Thompson, C. Verellen-Dumoulin, C. Laterre, 2004, Human Genetics.

Autoimmune thyroiditis associated with mild "subclinical" hypothyroidism in adults with Down syndrome: a comparison of patients with and without manifestations of Alzheimer disease.

M. Somerville, A. Dalton, M. Percy, 1990, American journal of medical genetics.

Evidence for the inheritance of silver-stained nucleolus organizer regions

R. Worton, V. Markovic, J. M. Berg, 1978, Human Genetics.

Family with 22-derived marker chromosome and late-onset dementia of the Alzheimer type: I. Application of a new model for estimation of the risk of disease associated with the marker.

M. Percy, D. Andrews, D. Crapper McLachlan, 1991, American journal of medical genetics.

Moving satellites and unstable chromosome translocations: clinical and cytogenetic implications.

V. Markovic, S. Farrell, E. Winsor, 1993, American journal of medical genetics.

Trisomy 15 mosaic derived from trisomic conceptus: report of a case and a review.

D. Chitayat, V. Markovic, B. Chodakowski, 1996, American journal of medical genetics.

Ecto-5'-nucleotidase. I. Expression in human normal and neoplastic lymphoid cell lines representing sequential stages of B-cell differentiation.

N. Sigal, T. Hibi, E. Gelfand, 1984, Journal of the National Cancer Institute.

Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother.

N. Simpson, R. Worton, R. Gardner, 1980, Journal of medical genetics.

Red cell superoxide dismutase, glutathione peroxidase and catalase in Down syndrome patients with and without manifestations of Alzheimer disease.

A. Dalton, M. Percy, D. Andrews, 1990, American journal of medical genetics.

Endocrine, cytogenetic and psychometric features of patients with X-isochromosome 46, X, i(Xq) Turner's syndrome: a preliminary study in nine patients.

B. Zinman, V. Markovic, J. Berg, 1984, Clinical and investigative medicine. Medecine clinique et experimentale.