[Syndrome 49,XXXXY,9qh+. Case report].

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

Back to search

Article

[Syndrome 49,XXXXY,9qh+. Case report].

Minerva pediatrica - 1 Apr 1994

Rocca M, Vivalda L, Bossi B, Spada M

Abstract excerpt

The case of a patient with 49, XXXXY, 9qh + syndrome is described. Father's karyotype is 46,XY,9qh+,9(qh +,inv(pllh12)).

Topics

Chromosome Aberrations
Chromosome Disorders
Cytogenetics
Humans
Infant
Karyotyping
Male
Parents
Phenotype

Source

Open in PubMed

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8084325

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-8084325-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation