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

Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation.

American journal of medical genetics. Part A - 1 Oct 2010

Razzaghian Hamid Reza, Shahi Mehdi Hayat, Forsberg Lars A, de Ståhl Teresita Diaz, Absher Devin, Dahl Niklas, Westerman Maxwell P, Dumanski Jan P

Abstract excerpt

Somatic genetic variation in health and disease is poorly explored. Monozygotic (MZ) twins are a suitable model for studies of somatic mosaicism since genetic differences in twins derived from the same zygote represent an irrefutable example of somatic variation. We report the analysis of a pair...

Read the complete abstract on PubMed

Topics

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

Share to Anemia, Sickle Cell
Share to Aneuploidy
Share to Chromosomes, Human, Pair 18

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, X

Share to Chromosomes, Human, Y

Share to Heterozygote

Share to Turner Syndrome

Share to Twins, Monozygotic

Source

Identifiers

PMID: 20734341
DOI: 10.1002/ajmg.a.33604

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20734341-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation.PMID 20734341Read ↗

Mosaicism in Human Health and Disease.Semantic proximity Read ↗

Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10,362 consecutive cases.Semantic proximity Read ↗

Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome.Semantic proximity Read ↗

Structural genetic variation in the context of somatic mosaicism.Semantic proximity Read ↗

Somatic Mosaicism in Biology and Disease.Semantic proximity Read ↗

A genomic view of mosaicism and human disease.Semantic proximity Read ↗

Somatic mosaicism in healthy human tissues.Semantic proximity Read ↗

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.Semantic proximity Read ↗

Mechanisms and consequences of somatic mosaicism in humans.Semantic proximity Read ↗

Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome.Semantic proximity Read ↗

Somatic mosaicism for copy number variation in differentiated human tissues.Semantic proximity Read ↗

Mosaic Turner syndrome shows reduced phenotypic penetrance in an adult population study compared to clinically ascertained casesSemantic proximity Read ↗

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