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Article

[Gonadal dysgenesis with karyotype 46 XY].

Annales d'endocrinologie - 1 Jan 2000

Guinet P

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

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PMID: 4311142

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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

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

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Gonadal dysgenesis with karyotype 46 XY].PMID 4311142Read ↗

[Gonadal asymmetry in intersex C, 46 XY karyotype].Semantic proximity Read ↗

Complete gonadal dysgenesis in clinical practice: the 46,XY karyotype accounts for more than one third of casesSemantic proximity Read ↗

[Karyotype 46, XX in a patient with a male phenotype].Semantic proximity Read ↗

[Normal development of the secondary sex characteristics in a case of 46,XY gonadal dysgenesis].Semantic proximity Read ↗

[47,XXY/46,XX mosaicism and abnormalities of sexual differentiation. A case report].Semantic proximity Read ↗

[46 XY--female phenotype: not just Morris syndrome].Semantic proximity Read ↗

[47 XXX karyotype in a phenotypically normal 22-year-old girl].Semantic proximity Read ↗

[Primary amenorrhea with XO-XY mosaicism and gonadoblastoma].Semantic proximity Read ↗

[A case of 46 XX gonadoblastoma].Semantic proximity Read ↗

[Analysis of two cases of Turner syndrome with 45,X/46,XY karyotype].Semantic proximity Read ↗

[Masculin phenotype in a child with a predominant 46, XX clone].Semantic proximity Read ↗

Clinical aspects of 49 infertile males with 45,X/46,XY mosaicism karyotype: A case series.Semantic proximity Read ↗

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