Cargando…

Prenatal diagnosis of a de novo interstitial deletion of 11q (11q22.3 → q23.3) associated with abnormal ultrasound findings by array comparative genomic hybridization

BACKGROUND: Conventional G-band karyotyping offers low-resolution detection of chromosome abnormalities and cannot provide information about the involved genomic content. On the other hand, array comparative genomic hybridization can offer a rapid and comprehensive detection of genomewide gains and...

Descripción completa

Detalles Bibliográficos
Autores principales:	Liu, Nian, Yan, Jiong, Chen, Xinlin, Song, Jieping, Wang, Bo, Yao, Yanyi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2014
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189608/ https://www.ncbi.nlm.nih.gov/pubmed/25298785 http://dx.doi.org/10.1186/s13039-014-0062-y

Ejemplares similares

de novo interstitial deletions at the 11q23.3-q24.2 region
por: Su, Jiasun, et al.
Publicado: (2016)

Clinical and molecular evaluations of siblings with “pure” 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3)
por: Chen, Rongyu, et al.
Publicado: (2014)

Annular pancreas in Trichorhinophalangeal syndrome type II with 8q23.3-q24.12 interstitial deletion
por: Li, Qi, et al.
Publicado: (2015)

A novel interstitial deletion of chromosome 2q21.1‐q23.3: Case report and literature review
por: Almuzzaini, Bader, et al.
Publicado: (2020)

Interstitial de novo 18q22.3q23 deletion: clinical, neuroradiological and molecular characterization of a new case and review of the literature
por: Tassano, Elisa, et al.
Publicado: (2016)

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy
por: Manolakos, Emmanouil, et al.
Publicado: (2011)

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy
por: Manolakos, Emmanouil, et al.
Publicado: (2011)

Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report
por: Krgovic, Danijela, et al.
Publicado: (2011)

Case Report: Candidate Genes Associated With Prenatal Ultrasound Anomalies in a Fetus With Prenatally Detected 1q23.3q31.2 Deletion
por: Song, Jiahao, et al.
Publicado: (2021)

An Interstitial Deletion at 10q26.2q26.3
por: Iourov, Ivan Y., et al.
Publicado: (2014)

23.3 DEVELOPMENTAL TRAJECTORIES OF SCHIZOPHRENIA-RELEVANT ABNORMALITIES IN A MOUSE MODEL OF 22Q11.2 DELETION SYNDROME
por: Ciampoli, Mariasole, et al.
Publicado: (2018)

Polymorphisms of the 11q23.3 Locus Affect the Risk and Mortality of Coronary Artery Disease
por: Iwanicki, Tomasz, et al.
Publicado: (2022)

A De Novo 8q22.2q22.3 Interstitial Microdeletion in a Girl with Developmental Delay and Congenital Defects
por: Kalinauskiene, Ruta, et al.
Publicado: (2023)

Narrowing down the region responsible for 1q23.3q24.1 microdeletion by identifying the smallest deletion
por: Hoshina, Takao, et al.
Publicado: (2019)

Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication
por: Libotte, Francesco, et al.
Publicado: (2021)

Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report
por: Mohammadi, Reza, et al.
Publicado: (2021)

Detection of 21q11.2‐q22.11 deletions in a fetus by NIPT
por: Zheng, Yunyun, et al.
Publicado: (2019)

Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case report
por: Ruiz-Botero, Felipe, et al.
Publicado: (2016)

Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers
por: Ghorbanoghli, Z., et al.
Publicado: (2016)

Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion.
por: Oh, Dong Chul, et al.
Publicado: (2002)

De novo deletion of chromosome 11q12.3 in monozygotic twins affected by Poland Syndrome
por: Vaccari, Carlotta Maria, et al.
Publicado: (2014)

A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization
por: Qi, Qingwei, et al.
Publicado: (2013)

A child with mosaicism for deletion (14)(q11.2q13)
por: Gamage, Thilini H., et al.
Publicado: (2012)

Chromosome 11q13 deletion syndrome
por: Kim, Yu-Seon, et al.
Publicado: (2016)

Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome
por: Heung, Tracy, et al.
Publicado: (2022)

Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH
por: Manolakos, Emmanouil, et al.
Publicado: (2013)

Interstitial duplication of 20q11.22q13.11: A case report and review of literature
por: Goetzinger, Logan, et al.
Publicado: (2021)

6q16.3q23.3 duplication associated with Prader-Willi-like syndrome
por: Desch, Laurent, et al.
Publicado: (2015)

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders
por: Isles, Anthony R., et al.
Publicado: (2016)

A common variant in 11q23.3 associated with hyperlipidemia is mediated by the binding and regulation of GATA4
por: Chou, Wen-Cheng, et al.
Publicado: (2022)

Cytogenetical and hematological analysis of chronic myelogenous leukemia patients with a novel case 52XX, t (1;9;22) (q23.3; q34; q11.2), +6, +8, i(9) (q10;q10), +18,+19,+21+der22 t(9;22)(q34;q11)
por: Asif, Muhammad, et al.
Publicado: (2022)

Phenotypic and genetic characterization of a patient with a de novo interstitial 14q24.1q24.3 deletion
por: Tassano, Elisa, et al.
Publicado: (2014)

An atypical 7Q11.2-Q21.11 deletion in a Williams-Beuren syndome patient
por: Lu, Wei, et al.
Publicado: (2013)

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk
por: Chang, Xiao, et al.
Publicado: (2017)

Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH
por: Shariati, Gholamreza, et al.
Publicado: (2018)

Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 gene
por: Luo, Man, et al.
Publicado: (2022)

Psychomotor retardation with a 1q42.11–q42.12 deletion
por: He, Jialing, et al.
Publicado: (2017)

Atypical 15q11.2-q13 Deletions and the Prader-Willi Phenotype
por: Grootjen, Lionne N., et al.
Publicado: (2022)

Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies
por: Su, Meng, et al.
Publicado: (2018)

Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotype
por: Song, Jieping, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_05hls21ri5drflojh0gmt8fb0j