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

Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome

1 Jan 2000

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 Epigenetics and DNA Methylation
Share to Genetic Syndromes and Imprinting
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10631135
DOI: 10.1086/302717

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

Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell SyndromePMID 10631135Read ↗

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.Semantic proximity Read ↗

Rare Causes and Differential Diagnosis in Patients With Silver-Russell Syndrome.Semantic proximity Read ↗

Approach to the Patient With Suspected Silver-Russell SyndromeSemantic proximity Read ↗

Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome.Semantic proximity Read ↗

New Developments in Silver–Russell Syndrome and Implications for Clinical PracticeSemantic proximity Read ↗

Cerebral visual impairment, autism, and pancreatitis associated with a 9 Mbp deletion on 10p12.Semantic proximity Read ↗

The next generation of Silver-Russell syndrome.Semantic proximity Read ↗

Silver-Russell Syndrome: A Review.Semantic proximity Read ↗

NSD1 duplication in Silver-Russell syndrome (SRS): molecular karyotyping in patients with SRS features.Semantic proximity Read ↗

Silver–Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1CSemantic proximity Read ↗

Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver–Russell syndromeSemantic proximity Read ↗

Report on 3 patients with 12p duplication including GRIN2BSemantic proximity Read ↗

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