TY  - JOUR
AU  - Đorđević, V. A.
AU  - Jovanović, J. V.
AU  - Pavković-Lucić, S. B.
AU  - Drakulić, Danijela
AU  - Đurović, M. M.
AU  - Gotić, M. D.
PY  - 2010
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/463
AB  - Cytogenetic findings are reported for 31 female patients with Turner's syndrome. Chromosome studies were made from lymphocyte cultures. Non-mosaicism 45, X was demonstrated in 15 of these patients, whereas only three were apparently mosaic. Eight patients showed non-mosaic and four patients showed mosaic structural aberrations of the X-chromosome. One non-mosaic case displayed a karyotype containing a small marker chromosome. Conventional cytogenetics was supplemented by fluorescence in situ hybridization (FISH) with an X-specific probe to identify the chromosomal origin of the ring and a 1q12-specific DNA probe to identify de novo balanced translocation (1;9) in one patient. To our knowledge, this is the first finding of karyotype 45,X,t(1;9) (cen;cen)/46,X,r(X),t(1;9)(cen;cen) in Turner's syndrome. The same X-specific probe was also used to identify a derivative chromosome in one patient.
PB  - FUNPEC-Editora, Ribeirao Preto
T2  - Genetics and Molecular Research
T1  - Cytogenetic findings in Serbian patients with Turner's syndrome stigmata
EP  - 2221
IS  - 4
SP  - 2213
VL  - 9
DO  - 10.4238/vol9-4gmr953
ER  - 

@article{
author = "Đorđević, V. A. and Jovanović, J. V. and Pavković-Lucić, S. B. and Drakulić, Danijela and Đurović, M. M. and Gotić, M. D.",
year = "2010",
abstract = "Cytogenetic findings are reported for 31 female patients with Turner's syndrome. Chromosome studies were made from lymphocyte cultures. Non-mosaicism 45, X was demonstrated in 15 of these patients, whereas only three were apparently mosaic. Eight patients showed non-mosaic and four patients showed mosaic structural aberrations of the X-chromosome. One non-mosaic case displayed a karyotype containing a small marker chromosome. Conventional cytogenetics was supplemented by fluorescence in situ hybridization (FISH) with an X-specific probe to identify the chromosomal origin of the ring and a 1q12-specific DNA probe to identify de novo balanced translocation (1;9) in one patient. To our knowledge, this is the first finding of karyotype 45,X,t(1;9) (cen;cen)/46,X,r(X),t(1;9)(cen;cen) in Turner's syndrome. The same X-specific probe was also used to identify a derivative chromosome in one patient.",
publisher = "FUNPEC-Editora, Ribeirao Preto",
journal = "Genetics and Molecular Research",
title = "Cytogenetic findings in Serbian patients with Turner's syndrome stigmata",
pages = "2221-2213",
number = "4",
volume = "9",
doi = "10.4238/vol9-4gmr953"
}

Đorđević, V. A., Jovanović, J. V., Pavković-Lucić, S. B., Drakulić, D., Đurović, M. M.,& Gotić, M. D.. (2010). Cytogenetic findings in Serbian patients with Turner's syndrome stigmata. in Genetics and Molecular Research
FUNPEC-Editora, Ribeirao Preto., 9(4), 2213-2221.
https://doi.org/10.4238/vol9-4gmr953

Đorđević VA, Jovanović JV, Pavković-Lucić SB, Drakulić D, Đurović MM, Gotić MD. Cytogenetic findings in Serbian patients with Turner's syndrome stigmata. in Genetics and Molecular Research. 2010;9(4):2213-2221.
doi:10.4238/vol9-4gmr953 .

Đorđević, V. A., Jovanović, J. V., Pavković-Lucić, S. B., Drakulić, Danijela, Đurović, M. M., Gotić, M. D., "Cytogenetic findings in Serbian patients with Turner's syndrome stigmata" in Genetics and Molecular Research, 9, no. 4 (2010):2213-2221,
https://doi.org/10.4238/vol9-4gmr953 . .