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

Paternal UPD14 with sSMC derived from chromosome 14 in Kagami-Ogata syndrome.

Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology - 19 Jan 2023

Wang Jiyong, Lichty Angie, Johnson Jill, Couick Chandler, Moore Mary Alice, Christensen Beth, Howard Khirston, Lee Jennifer A, DuPont Barbara R, Clarkson Lola, Hilton Benjamin A

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 Chromosome Disorders
Share to Chromosomes, Human, Pair 14
Share to Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Uniparental Disomy

Source

Identifiers

PMID: 36656404
DOI: 10.1007/s10577-023-09712-0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Paternal UPD14 with sSMC derived from chromosome 14 in Kagami-Ogata syndrome.PMID 36656404Read ↗

Paternal UPD14 with sSMC derived from chromosome 14 in Kagami-Ogata syndromeSemantic proximity Read ↗

Adults with paternal UPD14 causing Kagami-Ogata syndrome: Case report and review of the literature.Semantic proximity Read ↗

Uniparental disomy (UPD) other than 15: phenotypes and bibliography updated.Semantic proximity Read ↗

Derivative Complex Small Supernumerary Marker Chromosomes (sSMC) Involving Chromosome 2 and 15. A Novel Report.Semantic proximity Read ↗

Segmental and full paternal isodisomy for chromosome 14 in three patients: Narrowing the critical region and implication for the clinical featuresSemantic proximity Read ↗

An Incidental Detection of a Rare UPD in SNP-Array Based PGT-SR: A Case Report.Semantic proximity Read ↗

Abnormal phenotypes in uniparental disomy (UPD): fundamental aspects and a critical review with bibliography of UPD other than 15.Semantic proximity Read ↗

Small Supernumerary Marker Chromosomes and Uniparental Disomy Have a Story to TellSemantic proximity Read ↗

On the reported 8p22-p23.1 duplication in Kabuki make-up syndrome (KMS) and its absence in patients with typical KMS.Semantic proximity Read ↗

Maternal age effect on the development of Prader–Willi syndrome resulting from upd(15)mat through meiosis 1 errorsSemantic proximity Read ↗

A case report and mechanism analysis of a normal phenotype mosaic 47, XXY complicated by paternal iUPD (9) who had a normal PGD result.Semantic proximity Read ↗

Incidental finding of paternal UPD15 in a child with a deletion of 11q21-q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features.Semantic proximity Read ↗

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