TY  - JOUR
AU  - Damnjanović, Tatjana
AU  - Novaković, Ivana
AU  - Milašin, Jelena
AU  - Bunjevački, Vera
AU  - Jekić, Biljana
AU  - Cvijeticanin, Suzana
AU  - Luković, Ljiljana
PY  - 2007
UR  - https://smile.stomf.bg.ac.rs/handle/123456789/1365
AB  - The objective of this study was to assess indirectly the existence of X imprinting and its potential role in a number of clinical characteristics of Turner syndrome patients. Highly polymorphic X linked microsatellite markers were used to determine the origin of the single X chromosome in 13 patients with Turner syndrome. Ten (77%) patients retained the maternal X chromosome (X-m), while only three patients (23%) retained the paternal X chromosome (X-p). Fisher exact statistical test was used for the association of X chromosome origin with the clinical phenotype. No significant difference was found between the two groups of patients regarding the following phenotype characteristics: lymphoedema. at birth, short neck, low posterior hairline, eye anomalies (ptosis, epicanthal folds, hypertelorism, strabismus), multiple pigmented naevi, cardiac and renal anomalies. Absence association between the X chromosome origin and Turner phenotype was confirmed by a meta-analysis combining five studies, including this one. It was only neck webbing that showed a trend of association with X-m.
T2  - Korean Journal of Genetics
T1  - LeX chromosome imprinting in turner syndrome
VL  - 29
IS  - 3
SP  - 291
EP  - 295
UR  - https://hdl.handle.net/21.15107/rcub_smile_1365
ER  - 

@article{
author = "Damnjanović, Tatjana and Novaković, Ivana and Milašin, Jelena and Bunjevački, Vera and Jekić, Biljana and Cvijeticanin, Suzana and Luković, Ljiljana",
year = "2007",
abstract = "The objective of this study was to assess indirectly the existence of X imprinting and its potential role in a number of clinical characteristics of Turner syndrome patients. Highly polymorphic X linked microsatellite markers were used to determine the origin of the single X chromosome in 13 patients with Turner syndrome. Ten (77%) patients retained the maternal X chromosome (X-m), while only three patients (23%) retained the paternal X chromosome (X-p). Fisher exact statistical test was used for the association of X chromosome origin with the clinical phenotype. No significant difference was found between the two groups of patients regarding the following phenotype characteristics: lymphoedema. at birth, short neck, low posterior hairline, eye anomalies (ptosis, epicanthal folds, hypertelorism, strabismus), multiple pigmented naevi, cardiac and renal anomalies. Absence association between the X chromosome origin and Turner phenotype was confirmed by a meta-analysis combining five studies, including this one. It was only neck webbing that showed a trend of association with X-m.",
journal = "Korean Journal of Genetics",
title = "LeX chromosome imprinting in turner syndrome",
volume = "29",
number = "3",
pages = "291-295",
url = "https://hdl.handle.net/21.15107/rcub_smile_1365"
}

Damnjanović, T., Novaković, I., Milašin, J., Bunjevački, V., Jekić, B., Cvijeticanin, S.,& Luković, L.. (2007). LeX chromosome imprinting in turner syndrome. in Korean Journal of Genetics, 29(3), 291-295.
https://hdl.handle.net/21.15107/rcub_smile_1365

Damnjanović T, Novaković I, Milašin J, Bunjevački V, Jekić B, Cvijeticanin S, Luković L. LeX chromosome imprinting in turner syndrome. in Korean Journal of Genetics. 2007;29(3):291-295.
https://hdl.handle.net/21.15107/rcub_smile_1365 .

Damnjanović, Tatjana, Novaković, Ivana, Milašin, Jelena, Bunjevački, Vera, Jekić, Biljana, Cvijeticanin, Suzana, Luković, Ljiljana, "LeX chromosome imprinting in turner syndrome" in Korean Journal of Genetics, 29, no. 3 (2007):291-295,
https://hdl.handle.net/21.15107/rcub_smile_1365 .