Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review

19 Sept 2013

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics
Share to RNA modifications and cancer

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 24055730
DOI: 10.1016/j.gene.2013.09.044

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature reviewPMID 24055730Read ↗

Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.Semantic proximity Read ↗

Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal DiagnosisSemantic proximity Read ↗

Prenatal diagnosis, ultrasound findings, and pregnancy outcome of 17q12 deletion and duplication syndromes: a retrospective case series.Semantic proximity Read ↗

Clinical Findings and Genetic Analysis of Patients with Copy Number Variants Involving 17p13.3 By Using a Single Nucleotide Polymorphism Array: A Single-Center ExperienceSemantic proximity Read ↗

Expanding the phenotype of duplication of the Rubinstein-Taybi region on 16p13.3.Semantic proximity Read ↗

Practical guidelines for managing adults with 22q11.2 deletion syndromeSemantic proximity Read ↗

Prenatal diagnosis of complex phenotype in a 13-week-old fetus with an interstitial multigene deletion 20q13.13.-q13.2 by chromosomal microarray.Semantic proximity Read ↗

Road to A Rare Diagnosis: A Case Report Exploring Phenotype, Clinical Management and Outcome of a Rare and Novel Unbalanced Translocation causing complete Trisomy 17pSemantic proximity Read ↗

SCL19A3 gene mutation with Leigh-like phenotype presentation: a potentially treatable disease.Semantic proximity Read ↗

Prenatal diagnosis for chromosome abnormalities: past, present and futureSemantic proximity Read ↗

Practical Guidelines for Managing Patients with 22q11.2 Deletion SyndromeSemantic proximity Read ↗

Chromosomal Abnormality in Fetuses with Isolated Antenatal Hydronephrosis: Update for Prenatal Diagnosis and Genetic CounselingSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.