Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vjerica D. Markovic"'
Autor:
A.J. Dalton, Ann C. M. Rusk, Martin J. Somerville, Barbara Chodakowski, Joseph M. Berg, Donald R. McLachlan, David F. Andrews, Vjerica D. Markovic, Maire E. Percy
Publikováno v:
American Journal of Medical Genetics. 45:584-588
We previously observed low level mosaicism (2–4% normal cells) in phytohemagglutinin-stimulated peripheral blood lymphocytes (PBL) in 29% of a small group of elderly persons with Down syndrome (DS). An analysis of cytogenetic data on 154 trisomy 21
Autor:
Joseph M. Berg, Thomas G. Dearie, David F. Andrews, Maire E. Percy, Marlene E. Laing, Donald R. McLachlan, Jocelyn T. Hummel, Vjerica D. Markovic
Publikováno v:
American Journal of Medical Genetics. 39:307-313
We have identified 2 sisters with probable dementia of the Alzheimer type who have an unusual 22-derived marker chromosome with a greatly elongated short arm containing 2 well-separated nucleolus organizer regions. A marker chromosome similar in appe
Autor:
Maire E. Percy, Martin J. Somerville, David F. Andrews, D. R. Crapper McLachlan, Vjerica D. Markovic, Ann C. M. Rusk, A.J. Dalton, P. G. Walfish, Jocelyn T. Hummel, E. Gera
Publikováno v:
American journal of medical genetics. 36(2)
Serum tests of thyroid function were compared in Down syndrome (DS) patients with and without manifestations of Alzheimer disease (AD). Relative to control individuals, DS patients had, overall, lower mean total T4 (P = 0.070) and T3f (P = 0.015), hi
Autor:
Maire E. Percy, A.J. Dalton, Donald R. McLachlan, David F. Andrews, Jocelyn T. Hummel, Ann C. M. Rusk, Vjerica D. Markovic
Publikováno v:
American journal of medical genetics. 35(4)
The activities of red blood cell enzymes that scavenge the superoxide radical and hydrogen peroxide were measured in severely to profoundly retarded adult Down syndrome (DS) patients with and without manifestations of Alzheimer disease (AD), and cont
Publikováno v:
American journal of medical genetics. 20(1)
We report on a family in which an X;14 translocation has been identified. A phenotypically normal female, carrier of an apparently balanced X-autosome translocation t(X;14)(q22;q24.3) in all her cells and a small interstitial deletion of band 15q112