Cargando…

Cytogenetic Analysis of Sporadic First-Trimester Miscarriage Specimens Using Karyotyping and QF-PCR: A Retrospective Romanian Cohort Study

It is well known that first-trimester miscarriages are associated with chromosome abnormalities, with numerical chromosome abnormalities being the ones most commonly detected. Conventional karyotyping is still considered the gold standard in the analysis of products of conception, despite the extend...

Descripción completa

Detalles Bibliográficos
Autores principales:	Popescu-Hobeanu, Gabriela, Riza, Anca-Lelia, Streață, Ioana, Tudorache, Ștefania, Comănescu, Alexandru, Tănase, Florentina, Drăgușin, Roxana Cristina, Pascu, Cornelia, Dijmărescu, Anda Lorena, Cara, Monica-Laura, Dorobanțu, Ștefania, Petre-Mandache, Bianca, Cucu, Mihai, Sosoi, Simona Serban, Ioana, Mihai, Iliescu, Dominic, Burada, Florin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778060/ https://www.ncbi.nlm.nih.gov/pubmed/36553513 http://dx.doi.org/10.3390/genes13122246

Ejemplares similares

Phenotype Heterogeneity in 3q29 Microduplication Syndrome
por: STREATA, IOANA, et al.
Publicado: (2020)

Pathogenic Copy Number Variations Involved in the Genetic Etiology of Syndromic and Non-Syndromic Intellectual Disability—Data from a Romanian Cohort
por: Streață, Ioana, et al.
Publicado: (2022)

miR-499a rs3746444 A>G Polymorphism Is Correlated with Type 2 Diabetes Mellitus and Diabetic Polyneuropathy in a Romanian Cohort: A Preliminary Study
por: Burada, Emilia, et al.
Publicado: (2023)

Phenotypic and Genotypic Spectrum of Early-Onset Developmental and Epileptic Encephalopathies—Data from a Romanian Cohort
por: Riza, Anca-Lelia, et al.
Publicado: (2022)

Prenatal diagnosis of a pure 15q distal trisomy derived from a maternal pericentric inversion: A case report
por: Burada, Florin, et al.
Publicado: (2021)

Genetic Testing for Familial Hypercholesterolemia in a Pediatric Group: A Romanian Showcase
por: Constantin, Andreea Teodora, et al.
Publicado: (2023)

Association between genetic variants and depression in a Romanian cohort
por: Costache, Andrei, et al.
Publicado: (2021)

Characterization of sepsis inflammatory endotypes using circulatory proteins in patients with severe infection: a prospective cohort study
por: Ricaño-Ponce, Isis, et al.
Publicado: (2022)

First Trimester Ultrasound Detection of Fetal Central Nervous System Anomalies
por: Ungureanu, Delia Roxana, et al.
Publicado: (2023)

The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients
por: Budisteanu, Magdalena, et al.
Publicado: (2021)

Array CGH - A Powerful Tool in Molecular Diagnostic of Pathogenic Microdeletions - Williams-Beuren Syndrome - A Case Report
por: STREAȚĂ, I., et al.
Publicado: (2016)

The Association between Nod2 R702w Polymorphism and Susceptibility to Colorectal Cancer in Romanian Patients
por: BURADA, F., et al.
Publicado: (2018)

Prevalence and Predictors of Renal Disease in a National Representative Sample of the Romanian Adult Population: Data from the SEPHAR IV Survey
por: Pop, Călin, et al.
Publicado: (2022)

NOD2 Arg702Trp Polymorphism in Romanian Patients with Gastric Cancer
por: FLORESCU, D.N., et al.
Publicado: (2015)

Combination of QF‐PCR and aCGH is an efficient diagnostic strategy for the detection of chromosome aberrations in recurrent miscarriage
por: Lovrečić, Luca, et al.
Publicado: (2019)

ARG5 rs2245214 C/G Polymorphism Frequency in a Romanian Population
por: BURADA, F., et al.
Publicado: (2015)

PAH Pathogenic Variants and Clinical Correlations in a Group of Hyperphenylalaninemia Patients from North-Western Romania
por: Iuhas, Alin, et al.
Publicado: (2023)

Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene
por: Riza, Anca-Lelia, et al.
Publicado: (2022)

Quasi-Frobenius rings and generalizations QF-3 and QF-1 rings
por: Tachikawa, Hiroyuki
Publicado: (1973)

The psychiatric phenotype of 15q11.2-q13.3 duplications
por: Budisteanu, M., et al.
Publicado: (2021)

Autistic Behavior as Novel Clinical Finding in OFD1 Syndrome
por: Papuc, Sorina Mihaela, et al.
Publicado: (2023)

The Influence of the Variety, Vineyard, and Vintage on the Romanian White Wines Quality
por: Hosu, Anamaria, et al.
Publicado: (2016)

Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review
por: Kozma, Kinga, et al.
Publicado: (2021)

Specific lifestyle factors and in vitro fertilization outcomes in Romanian women: a pilot study
por: Neamtiu, Iulia A., et al.
Publicado: (2022)

Ageing People Living with HIV/AIDS, PLWHA; More Dental Challenges; the Romanian Dental Professional’s Point of View
por: Caministeanu, Florentina, et al.
Publicado: (2023)

Nasopharyngeal microbiota evaluation in three cohorts of children in the Romanian pediatric population
por: Streinu-Cercel, Anca, et al.
Publicado: (2014)

Susceptibility of Ocular Surface Bacteria to Various Antibiotic Agents in a Romanian Ophthalmology Clinic
por: Ghita, Aurelian Mihai, et al.
Publicado: (2023)

Workshop on Geometry, Topology, QF and Cosmology
Publicado: (2008)

Acceptability of Intrapartum Ultrasound Monitoring - Experience from a Romanian Longitudinal Study
por: ILIESCU, D.G., et al.
Publicado: (2015)

Periodontal disease in a young Romanian convenience sample: radiographic assessment
por: Hategan, Simona Ioana, et al.
Publicado: (2019)

Heart function assessment during aging in apolipoprotein E knock-out mice
por: Liehn, Elisa A., et al.
Publicado: (2021)

Some Information Measures Properties of the GOS-Concomitants from the FGM Family
por: Suter, Florentina, et al.
Publicado: (2022)

Determination of VEGFR-2 (KDR) 604A>G Polymorphism in Pancreatic Disorders
por: Pădureanu, Vlad, et al.
Publicado: (2017)

Prenatal findings and pregnancy outcome in fetuses with right and double aortic arch. A 10-year experience at a tertiary center
por: Petrescu, Ana-Maria, et al.
Publicado: (2020)

Voices of Romanian scientists
por: Stefania Pandolfi
Publicado: (2016)

Expanding the Clinical Phenotype of 19q Interstitial Deletions: A New Case with 19q13.32-q13.33 Deletion and Short Review of the Literature
por: Shelby, Elena-Silvia, et al.
Publicado: (2022)

COVID-19 and Laboratory Markers from Romanian Patients—A Narrative Review
por: Musat, Ovidiu, et al.
Publicado: (2023)

Serum Amino Acid Profiling in Children with Autistic Spectrum Disorder: Insights from a Single-Center Study in Southern Romania
por: Anastasescu, Cătălina Mihaela, et al.
Publicado: (2023)

Interleukin-4 Gene Polymorphisms in Romanian Patients with Inflammatory Bowel Diseases: Association with Disease Risk and Clinical Features
por: Ionescu, Elena Mirela, et al.
Publicado: (2023)

XRCC3 Thr241Met Polymorphism is not Associated with Lung Cancer Risk in a Romanian Population
por: CATANA, ANDREEA, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_pfnhb3f6a6s477gabu1bhgi94j