Found: 10
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Homologous Recombination Deficiency Score Determined by Genomic Instability in a Romanian Cohort.
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- Diagnostics (2075-4418), 2023, v. 13, n. 11, p. 1896, doi. 10.3390/diagnostics13111896
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- Article
Intrafamilial Phenotypical Variability Linked to PRKAG2 Mutation—Family Case Report and Review of the Literature.
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- Life (2075-1729), 2022, v. 12, n. 12, p. 2136, doi. 10.3390/life12122136
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- Article
Ovarian Cancer: Biomarkers and Targeted Therapy.
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- Biomedicines, 2021, v. 9, n. 6, p. 693, doi. 10.3390/biomedicines9060693
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- Article
Novel FHL1 mutation variant identified in a patient with nonobstructive hypertrophic cardiomyopathy and myopathy – a case report.
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- BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01131-w
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- Article
Sindromul malformației megalencefalo-capilare (MCAP).
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- Journal for Neurology & Psychiatry of Child & Adolescent in Romania, 2020, v. 26, n. 1, p. 45
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- Article
Chromosomal disorders and oro-dental defects - prenatal diagnosis.
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- Ginecologia.ro, 2019, v. 7, n. 24, p. 42, doi. 10.26416/gine.24.2.2019.2378
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- Article
A comprehensive analysis of genome-wide association studies to identify prostate cancer susceptibility loci for the Romanian population.
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- Romanian Journal of Morphology & Embryology, 2016, v. 57, n. 2, p. 467
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- Article
Receptorul și rolurile gonadotropinei corionice umane în sarcină.
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- Ginecologia.ro, 2016, v. 4, n. 11, p. 22
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- Article
Implicaţii genetice în tulburările din spectrul autismului.
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- Ginecologia.ro, 2015, v. 3, n. 10s, p. 29
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- Article
Distrofia musculară Duchenne perspective.
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- Ginecologia.ro, 2015, v. 3, n. 10s, p. 33
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- Article