Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Tsenghi C"'
Publikováno v:
American Journal of Medical Genetics. 38:437-439
The frequencies of autosomal folate sensitive fragile sites were compared in populations of mentally retarded fra(X) negative (N = 220) and normal children (N = 76) in Greece. In addition, the frequency of autosomal fragile sites was studied in 20 kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ac0c7d055d0416f1795092709c3ff81
https://doi.org/10.1002/ajmg.1320380259
https://doi.org/10.1002/ajmg.1320380259
The frequencies of autosomal folate sensitive fragile sites were compared in populations of mentally retarded fra(X) negative (N = 220) and normal children (N = 76) in Greece. In addition, the frequency of autosomal fragile sites was studied in 20 kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::1315fd00ca3364dcfc08fd2d261ed7d0
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3044251
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3044251
Publikováno v:
Acta Paediatrica; Jul1974, Vol. 63 Issue 4, p507-511, 5p
Autor:
Metaxotou, C., Ikkos, D., Panagiotopoulou, P., Alevizaki, M., Mavrou, A., Tsenghi, C., Matsaniotis, N.
Publikováno v:
Clinical Genetics; Nov1983, Vol. 24 Issue 5, p380-383, 4p
Autor:
N. Matsaniotis, Maria Alevizaki, P. Panagiotopoulou, Ariadni Mavrou, Tsenghi C, D. Ikkos, Catherine Metaxotou
Publikováno v:
Clinical Genetics. 24:380-383
A 14-year-old boy is described with hypogonadism, ichthyosis and mental retardation. His karyotype was 46,Y, der(X),t(X;)(p22;q11). His mother's karyotype was 46,X,der(X),t(X;Y)(p22;q11). Thus the son is nullisomic for the region Xp22 leads to pter a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8be4a7e126a35aefb7e9e6fe8ae40241
https://doi.org/10.1111/j.1399-0004.1983.tb00089.x
https://doi.org/10.1111/j.1399-0004.1983.tb00089.x
Publikováno v:
Pediatrics; August 1963, Vol. 32 Issue: 2 p272-279, 8p
We report on the first case of trisomy 3 detected in the lymphocytes of a live-born infant who died at the age of 5 months. A normal 46,XX karyotype was found in skin fibroblast cultures, which could account for the child's viability and lack of gros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::460cf63df81e828b2136b3b61c19b3f3
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3079310
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3079310
A cytogenetic investigation was carried out among 200 mentally retarded boys in Greece for the detection of the fragile X [fra(X)] syndrome. Thirteen patients were found to carry fra(X) (6.5%). Of those, six boys had a history of familial X-linked me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::c93954e92f5bb51487a11467fce5acff
http://olympias.lib.uoi.gr/jspui/handle/123456789/20181
http://olympias.lib.uoi.gr/jspui/handle/123456789/20181
The morphologic variations of C-band heterochromatin of chromosome 9 were studied in 600 Greek subjects referred for cytogenetic investigation. There was great variability in the location and length of the heterochromatic bands. The location and leng
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad9c22df8776094717ed77e0bf4d5d6a
https://europepmc.org/articles/PMC1685456/
https://europepmc.org/articles/PMC1685456/