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

A phenotypically normal female with pseudodicentric X: correlation for statural genes.

Singapore medical journal - 1 Sept 2001

Gole L A, Annapoorna V, Lim J, Anandakumar C

Abstract excerpt

A 14-year-old Chinese female presenting with primary amenorrhoea and poorly developed secondary sexual characteristics is described here. Cytogenetic analysis showed the presence of one normal X along with a dicentric X which had a duplication of the entire chromosome from the band Xp22.1 to Xqter. She was karyotyped as 46, XX, psu dic X (p22.1) (Xqter:Xp22.1::Xp22.1:Xqter), a variant of Turner syndrome. Both...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Body Height
Share to In Situ Hybridization, Fluorescence

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Karyotyping

Share to Phenotype

Share to Turner Syndrome

Share to X Chromosome

Source

Identifiers

PMID: 11811611

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A phenotypically normal female with pseudodicentric X: correlation for statural genes.PMID 11811611Read ↗

Pseudodicentric 22;Y translocation transmitted through four generations of a large family without phenotypic repercussion.Semantic proximity Read ↗

Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship?Semantic proximity Read ↗

Male with mosaicism for supernumerary ring X chromosome: analysis of phenotype and characterization of genotype using array comparative genome hybridization.Semantic proximity Read ↗

Karyotype-phenotype correlation in females with X chromosome abnormalities.Semantic proximity Read ↗

Cryptic Xp duplication including the SHOX gene in a woman with 46,X, del(X)(q21.31) and premature ovarian failureSemantic proximity Read ↗

The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.Semantic proximity Read ↗

Del(X)(p21.1) in a mother and two daughters: genotype-phenotype correlation of Turner features.Semantic proximity Read ↗

Disomy of distal Xq in males: case report and overview.Semantic proximity Read ↗

Klinefelter-like phenotype and primary infertility in a male with a paracentric Xq inversion.Semantic proximity Read ↗

Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patientsSemantic proximity Read ↗

Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X;Y translocationSemantic proximity Read ↗

Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation.Semantic proximity Read ↗

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