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Milena Stoyanova
Milena Stoyanova
在 mu-varna.bg 的电子邮件经过验证 - 首页
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The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered
J Brinkmann, C Lissewski, V Pinna, Y Vial, F Pantaleoni, F Lepri, ...
European Journal of Human Genetics 29 (3), 524-527, 2021
102021
Comparison between thrombophilic gene polymorphisms among high risk patients
M Levkova, M Hachmeriyan, M Stoyanova, V Miteva, L Angelova
Romanian Journal of Internal Medicine 58 (1), 20-26, 2020
82020
Maternal biochemical screening – an approach for genetic prevention. Part 2.Sequential approach with integrated risk assessment
L Angelova, V Gadancheva, D Konstantinova, M Stoianova, ...
Akusherstvo I Ginekologia (indexed in Medline) 52 (5), 14-18, 2013
62013
Standard karyotyping-a look through the European guidelines
M Hachmeriyan, M Levkova, M Stoyanova, V Miteva, L Angelova
Varna Medical Forum 8 (1), 90-96, 2019
42019
16p11. 2 Duplication Syndrome-a Case Report
M Levkova, M Stoyanova, R Staneva, M Hachmeriyan, L Angelova
Folia Medica 63 (1), 138-141, 2021
32021
Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour
S Milena, H Mari, L Mariya, B Stoyan, G Miglena, M Vilhelm, L Angelova
Folia Medica 64 (1), 27-32, 2022
22022
Women’s awareness towards prenatal Down syndrome tests in Bulgaria.
LA Levkova M., M. Hachmeriyan, V. Miteva, M. Stoyanova, M. Tsvetkova, D ...
Journal of Down Syndrome and Chromosome Abnormalities 4 (2), 2018
22018
Challenging Reproductive Genetic Counseling in Families at High Risk for Rare Genetic Syndromes – A Case Report with Possible Denys-Drash Syndrome
AL Hachmeriyan M., Andonova S., Levkova M.,Stoyanova M., Kalchev K., Vasilev ...
Journal of Genetic Disorders & Genetic Reports 7 (1), 2018
2*2018
Diagnosis of the socionic temperament of personality and creating a psychological portrait of the Western European SPA and wellness tourists in Bulgaria
M Stoyanova
Acta Scientifica Naturalis 4 (1), 84-88, 2017
22017
Tendencies of cytogenetic analysis of patients with acute myeloid leukemia–an 11-year single-centre experience report
D Yahya, T Ruseva, M Tsvetkova, M Stoyanova, M Levkova, V Miteva, ...
2
Variants of uncertain significance in the era of next-generation sequencing
M Levkova, M Stoyanova, M Benkova-Petrova, M Georgieva, L Angelova
Journal of the American Association of Nurse Practitioners 34 (8), 1018-1021, 2022
12022
The application of the facial analysis program Face2Gene in a single genetic counseling center: a retrospective study
D Yahya, M Stoyanova, M Hachmeriyan, M Levkova
Egyptian Pediatric Association Gazette 73 (1), 1, 2025
2025
NIPT Integration as a Patient-Paid Prenatal Screening Option—Observations and Challenges from a Bulgarian Genetic Counseling Center
D Yahya, M Hachmeriyan, M Stoyanova, M Levkova
Medical Sciences 13 (1), 3, 2024
2024
A cost-efficient algorithm for diagnosing children with dysmorphic features
M Levkova, M Stoyanova, M Hachmeriyan, L Angelova
Egyptian Journal of Medical Human Genetics 25 (1), 76, 2024
2024
The significance of follow-up in patients with dysmorphic features: a case from clinical practice
M Levkova, M Stoyanova, M Hachmeriyan
Romanian JouRnal of PediatRics 73 (2), 100, 2024
2024
HEREDITARY BREAST AND OVARIAN CANCER–GENETIC COUNSELING EXPERIENCE REPORT
D Yahya, M Hachmeriyan, V MITEVA, M STOYANOVA, M Levkova, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 339-339, 2024
2024
ACAN gene mutation in a patient born small for gestational age with familial short stature
V Iotova, Y Deyanova, M Stoyanova, M Hachmeriyan
HORMONE RESEARCH IN PAEDIATRICS 96, 338-338, 2023
2023
Noonan syndrome patients with short stature at a single paediatric endocrinology centre
Y Deyanova, V Iotova, M Stoyanova, I Halvadzhiyan, R Stoicheva, ...
Scripta Scientifica Medica 54 (3), 21-26, 2022
2022
Molecular genetic markers in acute myelogenous leukemia—the good, the bad, and the intermediate
DA Yahya, M Hachmeriyan, M Stoyanova, L Angelova, I Micheva, ...
Varna Medical Forum 11 (2), 7-19, 2022
2022
Telegenetics: attitudes of genetic counselors and patients in Bulgaria
M Levkova, M Hachmeriyan, M Stoyanova, V Miteva, L Angelova
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 570-570, 2022
2022
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