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

Implications of prenatal diagnosis of the fetus with both interstitial deletion and a small marker ring originating from chromosome 5.

American journal of medical genetics. Part A - 1 Jan 2011

Ohashi Hiroyasu, Suzumori Kaoru, Chisaka Yasushi, Sonta Shinichi, Kobayashi Tomoko, Aoki Yoko, Matsubara Yoichi, Sone Michiko, Shaffer Lisa G

Abstract excerpt

We describe a patient with 47,XY,del(5)(p11p13), +mar observed in prenatal screening. We performed analyses including G-banding, multi-color fluorescent in situ hybridization (mFISH) for fetal chromosome detection. After birth array-based comparative genomic hybridization (aCGH), bacterial artifi...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Deletion
Share to Chromosomes, Artificial, Bacterial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 5

Share to Comparative Genomic Hybridization

Share to In Situ Hybridization, Fluorescence

Share to Ring Chromosomes

Share to Trisomy

Source

Identifiers

PMID: 21204231
DOI: 10.1002/ajmg.a.33764

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21204231-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Implications of prenatal diagnosis of the fetus with both interstitial deletion and a small marker ring originating from chromosome 5.PMID 21204231Read ↗

[Study of two cases of prenatally detected small supernumerary marker chromosomes].Semantic proximity Read ↗

[Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array].Semantic proximity Read ↗

Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication.Semantic proximity Read ↗

40 Mb duplication in chromosome band 5p13.1p15.33 with 800 kb terminal deletion in a foetus with mild phenotypic features.Semantic proximity Read ↗

Molecular characterisation of a prenatally diagnosed 5q15q21.3 deletion and review of the literature.Semantic proximity Read ↗

[Phenotypic and genetic analysis of a child featuring multiple malformations due to copy number variation on chromosome 5].Semantic proximity Read ↗

Molecular cytogenetic and clinical characterization of a patient with a 5.6-Mb deletion in 7p15 including HOXA cluster.Semantic proximity Read ↗

[Prenatal diagnosis of a tetrasomy 18p case using BACs-on-Beads technology and single nucleotide polymorphism array].Semantic proximity Read ↗

A report on seven fetal cases associated with 15q11-q13 microdeletion and microduplication.Semantic proximity Read ↗

[Prenatal diagnosis of three fetuses with small supernumerary marker chromosomes].Semantic proximity Read ↗

Prenatal diagnosis of a 15q24.1 microdeletion in a fetus with cerebral and urogenital abnormalities.Semantic proximity Read ↗

Sperm and Embryo Analysis in a Carrier of Supernumerary inv dup(15) Marker ChromosomeSemantic proximity Read ↗

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