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Article

[Familial male pseudohermaphroditism].

La Revue francaise d'endocrinologie clinique, nutrition, et metabolisme - 1 Jan 2000

Milcou S M, Serban A M, Ionesco B, Simionesco N, Maximilian C

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

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PMID: 5731398

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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.

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[Familial male pseudohermaphroditism].PMID 5731398Read ↗

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Male pseudohermaphroditism caused by mutations of the human androgen receptor.Semantic proximity Read ↗

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[Male pseudohermaphroditism due to disorder of androgen receptor function].Semantic proximity Read ↗

[Male pseudohermaphroditism. State and present problems (author's transl)].Semantic proximity Read ↗

Phenotypically normal girl with male pseudohermaphroditism, hypoplastic left ventricle, lung aplasia, horseshoe kidney, and diaphragmatic hernia.Semantic proximity Read ↗

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[Causative genetic variants of pseudohypoaldosteronism type II and essential hypertension].Semantic proximity Read ↗

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