Cargando…

Investigation of Genetic Alterations in Congenital Heart Diseases in Prenatal Period

The prenatal diagnosis of congenital heart disease (CHD) is important because of mortality risk. The onset of CHD varies, and depending on the malformation type, the risk of aneuploidy is changed. To identify possible genetic alterations in CHD, G-banding, chromosomal microarray or if needed DNA mut...

Descripción completa

Detalles Bibliográficos
Autores principales:	Atli, Emine Ikbal, Atli, Engin, Yalcintepe, Sinem, Demir, Selma, Kalkan, Rasime, Akurut, Cisem, Ozen, Yasemin, Gurkan, Hakan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Georg Thieme Verlag KG 2021
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837410/ https://www.ncbi.nlm.nih.gov/pubmed/35169781 http://dx.doi.org/10.1055/s-0041-1736566

Ejemplares similares

Clinical Features of Aberrations Chromosome 22q: A Pilot Study
por: Atli, Emine Ikbal, et al.
Publicado: (2021)

The Importance of Targeted Next-Generation Sequencing Usage in Cytogenetically Normal Myeloid Malignancies
por: Atli, Emine Ikbal, et al.
Publicado: (2021)

Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype
por: Zhuri, Drenushe, et al.
Publicado: (2022)

The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method
por: Yalcintepe, Sinem, et al.
Publicado: (2023)

Two Novel Pathogenic FBN1 Variations and Their Phenotypic Relationship of Marfan Syndrome
por: Yalcintepe, Sinem, et al.
Publicado: (2020)

Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique
por: Atlı, Engin, et al.
Publicado: (2023)

Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes
por: YALÇINTEPE, Sinem, et al.
Publicado: (2021)

Comprehensive Genetic Analysis Results of TSC1/TSC2 Genes in Patients with Clinical Suspicion of Tuberous Sclerosis Complex and Definition of 3 Novel Variants
por: Demir, Selma, et al.
Publicado: (2021)

The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region
por: Yalçıntepe, Sinem, et al.
Publicado: (2021)

Investigating the Genetic Etiology of Pediatric Patients with Peripheral Hypotonia Using the Next-Generation Sequencing Method
por: Eker, Damla, et al.
Publicado: (2022)

Pros and Cons for Fluorescent in Situ Hybridization, Karyotyping and Next Generation Sequencing for Diagnosis and Follow-up of Multiple Myeloma
por: Ikbal Atli, E, et al.
Publicado: (2021)

Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma
por: Yalcintepe, Sinem, et al.
Publicado: (2021)

Two Cases of Cystic Fibrosis with Compound Heterozygous Variants Reported for the First Time
por: Yalçıntepe, Sinem, et al.
Publicado: (2020)

Concepts of Double Hit and Triple Hit Disease in Multiple Myeloma, Entity and Prognostic Significance
por: Baysal, Mehmet, et al.
Publicado: (2020)

A 9-Year-Old-Girl with Phelan McDermid Syndrome, Who Had been Diagnosed with an Autism Spectrum Disorder
por: Görker, I, et al.
Publicado: (2016)

Investigation of Genes Associated With Atherosclerosis in Patients With Systemic Lupus Erythematosus
por: BALCI, Mehmet Ali, et al.
Publicado: (2021)

Multiple Inherited Thrombophilic Gene Polymorphisms in Spontaneous Abortions in Turkish Population
por: Yalcintepe, Sinem, et al.
Publicado: (2015)

Prenatal Diagnosis of a New Case: De Novo Balanced Non-Robertsonian Translocation Involving t(15;22)(p11.2;q11.2)
por: Atli, Eİ, et al.
Publicado: (2018)

Investigation of The Relationship of TNFRSF11A Gene Polymorphisms with Breast Cancer Development and Metastasis Risk in Patients with BRCA1 Or BRCA2 Pathogenic Variants Living in The Trakya Region of Turkey
por: Özdemir, K, et al.
Publicado: (2021)

A case with Emanuel syndrome: extra derivative 22 chromosome inherited from the mother
por: İkbal Atli, E, et al.
Publicado: (2016)

Synthesis, characterization and catalytic properties of cationic N-heterocyclic carbene silver complexes
por: DEMİR ATLI, Deniz
Publicado: (2021)

Determining the linear correlation between dielectric spectroscopy and viable biomass concentration in filamentous fungal fermentations
por: Magnússon, Atli, et al.
Publicado: (2023)

Genetic and Epigenetic Alterations in Autism Spectrum Disorder
por: Oztenekecioglu, Bugsem, et al.
Publicado: (2021)

Matrix metalloproteinases are possible targets in monocrotaline-induced pulmonary hypertension: investigation of anti-remodeling effects of alagebrium and everolimus
por: Atlı, Özlem, et al.
Publicado: (2017)

Glioblastoma Stem Cells as a New Therapeutic Target for Glioblastoma
por: Kalkan, Rasime
Publicado: (2015)

Epigenetic Alteration in Colorectal Cancer: A Biomarker for Diagnostic and Therapeutic Application
por: Essa, Hafsa Yousif Solayman, et al.
Publicado: (2022)

Assessment of COVID-19 trauma responses. Who has been more traumatized during the pandemic?
por: Akyuz Cim, Emine Fusun, et al.
Publicado: (2022)

The investigation of factors related to suicide attempts in Southeastern Turkey
por: Okan Ibiloglu, Aslihan, et al.
Publicado: (2016)

Acute and Subchronic Toxic Effects of the Fruits of Physalis peruviana L.
por: Perk, Basak Ozlem, et al.
Publicado: (2013)

Reproductive toxicity after levetiracetam administration in male rats: Evidence for role of hormonal status and oxidative stress
por: Baysal, Merve, et al.
Publicado: (2017)

Cancer Treatment: An Epigenetic View
por: Aydin, Cansu, et al.
Publicado: (2020)

Epigenetic Approach to PTSD: In the Aspects of Rat Models
por: Aykac, Asli, et al.
Publicado: (2021)

A New Perspective of COVID-19 Infection: An Epigenetics Point of View
por: Ozturkler, Ziya, et al.
Publicado: (2021)

The efficiency of cinacalcet treatment in delaying parathyroidectomy in a case with neonatal severe hyperparathyroidism caused by homozygous mutation in the CASR gene
por: Çömlek, Fatma Özgüç, et al.
Publicado: (2022)

Spectral-spatial classification of hyperspectral remote sensing images
por: Benediktsson, Jon Atli, et al.
Publicado: (2015)

Postural Asymmetries and Assistive Devices Used by Adults With Cerebral Palsy in Lying, Sitting, and Standing
por: Rodby-Bousquet, Elisabet, et al.
Publicado: (2021)

Sertraline-induced reproductive toxicity in male rats: evaluation of possible underlying mechanisms
por: Atli, Ozlem, et al.
Publicado: (2017)

Toxic Effects of Trazodone on Male Reproductive System via Disrupting Hypothalamic-Pituitary-Testicular Axis and Inducing Testicular Oxidative Stress
por: Ilgın, Sinem, et al.
Publicado: (2018)

Corrigendum to “Toxic Effects of Trazodone on Male Reproductive System via Disrupting Hypothalamic-Pituitary-Testicular Axis and Inducing Testicular Oxidative Stress”
por: Ilgın, Sinem, et al.
Publicado: (2018)

Trace elements and organic contaminants in tissues of minke whale (Balaenoptera acutorotstrata) and its feed from Icelandic waters
por: Auðunsson, Guðjón Atli, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_fk47hkgkrm584mv5s0e5rcnu6b