Cargando…

Application of array comparative genomic hybridization in Korean children under 6 years old with global developmental delay

PURPOSE: Recent advancements in molecular techniques have greatly contributed to the discovery of genetic causes of unexplained developmental delay. Here, we describe the results of array comparative genomic hybridization (CGH) and the clinical features of 27 patients with global developmental delay...

Descripción completa

Detalles Bibliográficos
Autores principales:	Lee, Kyung Yeon, Shin, Eunsim
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Pediatric Society 2017
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638834/ https://www.ncbi.nlm.nih.gov/pubmed/29042871 http://dx.doi.org/10.3345/kjp.2017.60.9.282

Ejemplares similares

1p36 deletion syndrome confirmed by fluorescence in situ hybridization and array-comparative genomic hybridization analysis
por: Kang, Dong Soo, et al.
Publicado: (2016)

Application of Array-Based Comparative Genomic Hybridization to Pediatric Neurologic Diseases
por: Byeon, Jung Hye, et al.
Publicado: (2014)

Array-Based Comparative Genomic Hybridization in 190 Korean Patients with Developmental Delay and/or Intellectual Disability: A Single Tertiary Care University Center Study
por: Lee, Cha Gon, et al.
Publicado: (2013)

Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability
por: Bartnik, Magdalena, et al.
Publicado: (2013)

Array-Based Comparative Genomic Hybridization Analysis in Children with Developmental Delay/Intellectual Disability
por: Türkyılmaz, A, et al.
Publicado: (2022)

Application of array comparative genomic hybridization (array- CGH) for detection of chromosomal imbalances in children with developmental delay/congenital malformations in Saudi Arabia
por: Hussein, Ibtessam Ramzi, et al.
Publicado: (2014)

A structural MRI study of global developmental delay in infants (<2 years old)
por: Sun, Hui-miao, et al.
Publicado: (2022)

SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay
por: D’Amours, Guylaine, et al.
Publicado: (2014)

Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
por: Papadopoulou, Zoe, et al.
Publicado: (2017)

The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay
por: Wayhelova, Marketa, et al.
Publicado: (2019)

A new mosaic der(18)t(1;18)(q32.1;q21.3) with developmental delay and facial dysmorphism
por: Choi, Young-Jin, et al.
Publicado: (2016)

Clinical Usefulness of the Korean Developmental Screening Test (K-DST) for Developmental Delays
por: Jang, Chul Hoon, et al.
Publicado: (2019)

Predictors of Developmental Outcome in 4- to 6-Year-Olds With Developmental Disability
por: Lee, Taeyeop, et al.
Publicado: (2022)

Vocalization of Emotional and Social Expressions in Korean-Speaking Toddlers with Autism Spectrum Disorder and Those with Developmental Delay
por: Lee, Kyung-Sook, et al.
Publicado: (2018)

Metabolic evaluation of children with global developmental delay
por: Eun, So-Hee, et al.
Publicado: (2015)

The use of array-CGH in a cohort of Greek children with developmental delay
por: Manolakos, Emmanouil, et al.
Publicado: (2010)

Routine Chromosomal Microarray Analysis is Necessary in Korean Patients With Unexplained Developmental Delay/Mental Retardation/Autism Spectrum Disorder
por: Shin, Saeam, et al.
Publicado: (2015)

Prevalence and Developmental Profiles of Autism Spectrum Disorders in Children With Global Developmental Delay
por: Shan, Ling, et al.
Publicado: (2022)

Diagnosis of Schaaf-Yang syndrome in Korean children with developmental delay and hypotonia
por: Ahn, Hyunji, et al.
Publicado: (2020)

Delayed processing of global shape information in developmental prosopagnosia
por: Gerlach, Christian, et al.
Publicado: (2017)

Familial Global Developmental Delay Secondary to β-Mannosidosis
por: Gowda, Vykuntaraju K., et al.
Publicado: (2021)

Usefulness of the Korean Developmental Screening Test for infants and children for the evaluation of developmental delay in Korean infants and children: a single-center study
por: Yim, Chung-Hyuk, et al.
Publicado: (2017)

De novo interstitial deletion of 15q22q23 with global developmental delay and hypotonia: the first Korean case
por: Kim, Ha-Su, et al.
Publicado: (2015)

Targeted Next-Generation Sequencing of Korean Patients With Developmental Delay and/or Intellectual Disability
por: Han, Ji Yoon, et al.
Publicado: (2018)

Lower palatine developmental instability in hybrid Old World camelids
por: Parés-Casanova, Pere M., et al.
Publicado: (2020)

Refractory seizures with global developmental delay: A rare cause
por: Vinoth, P. N., et al.
Publicado: (2011)

CNS Structural Anomalies in Iranian Children with Global Developmental Delay
por: ZAMANI, Gholam Reza, et al.
Publicado: (2013)

Etiological Yield of Global Developmental Delay in Kanti Children's Hospital
por: Jha, Anshu
Publicado: (2018)

Genetic architecture and temporal analysis of Caenorhabditis briggsae hybrid developmental delay
por: Velazco-Cruz, Leonardo, et al.
Publicado: (2022)

Correlation of Language Assessment Batteries of Toddlers With Developmental Language Delay
por: Yoon, Jin A, et al.
Publicado: (2022)

A Comparison of the Korean-Ages and Stages Questionnaires and Denver Developmental Delay Screening Test
por: Ga, Hyo-yun, et al.
Publicado: (2011)

Importance of Genetic Diagnosis in Global Developmental Delay: A Case of Cabezas Syndrome Caused by CUL4B Gene Deletion and Not Identified by Array-CHG
por: Magalhães, Teresa L, et al.
Publicado: (2023)

Current evidence-based recommendations on investigating children with global developmental delay
por: Mithyantha, Renuka, et al.
Publicado: (2017)

Oral Health Characteristics and Dental Rehabilitation of Children with Global Developmental Delay
por: Kumar, Saurabh, et al.
Publicado: (2017)

Evaluation of Individuals with Non-Syndromic Global Developmental Delay and Intellectual Disability
por: AlMutiri, Rowim, et al.
Publicado: (2023)

Computational Methods for the Analysis of Array Comparative Genomic Hybridization
por: Chari, Raj, et al.
Publicado: (2007)

Application of array-comparative genomic hybridization in tetralogy of Fallot
por: Liu, Lin, et al.
Publicado: (2016)

Developmental heatmaps of brain functional connectivity from newborns to 6-year-olds
por: Chen, Haitao, et al.
Publicado: (2021)

Social developmental delays among 3 to 6 year old children in preschools in German social hotspots: results of a dynamic prospective cohort study
por: Biermann, Josefin, et al.
Publicado: (2020)

Erratum: A Comparison of the Korean-Ages and Stages Questionnaires and Denver Developmental Delay Screening Test
Publicado: (2011)

Cannot write session to /tmp/vufind_sessions/sess_5mtvc99a03437tn0983d8bct4h