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

Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype.

Journal of medical genetics - 1 Aug 1999

Bijlsma E K, Aalfs C M, Sluitjer S, Oude Luttikhuis M E, Trembath R C, Hoovers J M, Hennekam R C

Abstract excerpt

Recently five patients with an Albright hereditary osteodystrophy (AHO)-like phenotype were reported to have a subtelomeric deletion of the long arm of chromosome 2. These patients showed a striking resemblance to a number of patients from a large pedigree known to us for a long time. After molec...

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, Human, Pair 2
Share to Chromosomes, Human, Pair 8

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fibrous Dysplasia, Polyostotic

Share to In Situ Hybridization, Fluorescence

Share to Karyotyping

Share to Radiography

Share to Translocation, Genetic

Source

Open in PubMed Open full text

Identifiers

PMID: 10465110
PMCID: PMC1762967

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-10465110-2026-09-04.2. 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

Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype.PMID 10465110Read ↗

Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype.Semantic proximity Read ↗

A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype.Semantic proximity Read ↗

2q37.3 Deletion Syndrome: Two Cases with Highly Distinctive Facial Phenotype, Discordant Association with Schizophrenic Psychosis, and Shared Deletion Breakpoint Region on 2q37.3.Semantic proximity Read ↗

Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype.Semantic proximity Read ↗

A cryptic unbalanced translocation t(2;9)(p25.2;q34.3) causes the phenotype of 9q subtelomeric deletion syndrome and additional exophthalmos and joint contractures.Semantic proximity Read ↗

Chromosome 2q37 deletion: clinical and molecular aspects.Semantic proximity Read ↗

[Clinical manifestation of chromosome 2 long arm terminal deletion--presentation of four cases].Semantic proximity Read ↗

Pure distal trisomy 2q: a rare chromosomal abnormality with recognizable phenotype.Semantic proximity Read ↗

Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.Semantic proximity Read ↗

Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy.Semantic proximity Read ↗

2q31.2q32.3 deletion syndrome: report of an adult patient.Semantic proximity Read ↗

Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.Semantic proximity Read ↗

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