المؤلفون: Sleptsova M, Georgiev C, Atemin S, Dimova P, Avdjieva-Tzavella D, Tacheva G, Litvinenko I, Grozdanova L, Todorov T, Mitev V, Todorova A

المصدر: Balkan Journal of Medical Genetics, Vol 26, Iss 2, Pp 65-68 (2024)

مصطلحات موضوعية: epha4, whole exome sequencing, epilepsy, novel genetic variant, ophthalmological anomalies, neurodevelopmental delay, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2199-5761

URL الوصول: https://doaj.org/article/803898290e104d83b60c1ceb8311e0c3

المؤلفون: Sleptsova, M, Georgiev, C, Atemin, S, Dimova, P, Avdjieva-Tzavella, D, Tacheva, G, Litvinenko, I, Grozdanova, L, Todorov, T, Mitev, V, Todorova, A

المصدر: Balkan Journal of Medical Genetics; March 2024, Vol. 26 Issue: 2 p65-68, 4p

المؤلفون: Sleptsova, M, Georgiev, C, Atemin, S, Dimova, P, Avdjieva-Tzavella, D, Tacheva, G, Litvinenko, I, Grozdanova, L, Todorov, T, Mitev, V, Todorova, A

المصدر: Balkan Journal of Medical Genetics; Dec2023, Vol. 26 Issue 2, p65-68, 4p

مصطلحات موضوعية: GENETIC variation, PEOPLE with epilepsy, SPERM donation, NEURAL development, GENETIC testing

المؤلفون: Hadil Kathom, Avdjieva-Tzavella, D., Sinigerska, I., Ivanova, M., Tacheva, G., Stamatov, D., Bojidarova, M., Litvinenko, I., Tincheva, R.

المصدر: Scopus-Elsevier

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::10b63c0b5d4a64c342a643d2c7c841e2
http://www.scopus.com/inward/record.url?eid=2-s2.0-85009200835&partnerID=MN8TOARS