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Article

Unusual clinical syndrome in a boy with 45,X/46,XY mosaicism.

Genetic counseling (Geneva, Switzerland) - 1 Jan 2005

Lespinasse J, Murthy S, Lesca G, Palfreeman N, Lemeyre E

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

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Identifiers

PMID: 15844789

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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

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Unusual clinical syndrome in a boy with 45,X/46,XY mosaicism.PMID 15844789Read ↗

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Clinicopathological features of 45,X/46,Xidic(Y) mosaicism and therapeutic implications: case report.Semantic proximity Read ↗

45,X/47,XYY mosaicism: Clinical discrepancy between prenatally and postnatally diagnosed casesSemantic proximity Read ↗

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Ullrich-Turner phenotype with unusual manifestation in a patient with mosaicism 45,X/47,XX,+18.Semantic proximity Read ↗

Syndrome X: clinical aspects.Semantic proximity Read ↗

High-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a fetus with a favorable fetal outcome and the karyotype of 46,XX in the neonatal peripheral blood at age 4½ monthsSemantic proximity Read ↗

45,X/46,XY mosaicism: report on 14 patients from a Brazilian hospital. A retrospective study.Semantic proximity Read ↗

Unusual endocrine and somatic phenotypic abnormalities in a 14-year-old boy with classic Klinefelter syndrome (47,XXY).Semantic proximity Read ↗

45,X/46,XY mosaicism and fragile X syndrome.Semantic proximity Read ↗

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