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Milena Stoyanova
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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
72021
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
62020
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
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
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
16p11. 2 Duplication Syndrome-a Case Report
M Levkova, M Stoyanova, R Staneva, M Hachmeriyan, L Angelova
Folia Medica 63 (1), 138-141, 2021
12021
Hereditary breast and ovarian cancer-genetic counseling experience report
D Yahya, M Hachmeriyan, M Stoyanova, V Miteva, 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
COVID-19 effect on post-test genetic counselling
M Hachmeriyan, M Levkova, D Yahya, M Stoyanova, V Miteva, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 561-561, 2022
2022
Evaluation of the diagnostic rate in children with dysmorphic features-one genetic center experience
M Stoyanova, M Hachmeriyan, M Levkova, V Miteva, L Angelova
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 338-338, 2022
2022
Incidental findings in cytogenetics-the old new
V Miteva, T Ruseva, D Yahya, M Levkova, M Stoyanova, M Hachmeryan, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 560-561, 2022
2022
Genetic Diagnostic Study Among Pediatric Patients with Hereditary Pathology Who Received Genetic Counselling
MP Stoyanova
PQDT-Global, 2022
2022
Practical aspects and effectiveness of genetic counseling in children with hereditary pathologies
M Stoyanova, L Angelova, M Levkova, M Georgieva, V Iotova
General Medicine 24 (1), 30-36, 2022
2022
Noonan syndrome patients with short stature at a single pediatric endocrinology centre
Y Deyanova, V Iotova, K Tsochev, M Stoyanova, R Stoicheva, V Mladenov, ...
HORMONE RESEARCH IN PAEDIATRICS 94 (SUPPL 1), 338-339, 2021
2021
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