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Article

Prenatal diagnosis of 46,XX male fetuses.

American journal of obstetrics and gynecology - 1 Apr 1999

Ginsberg N A, Cadkin A, Strom C, Bauer-Marsh E, Verlinsky Y

Abstract excerpt

Ultrasonography can accurately determine phenotypic sex differences from those of the genetic sex. Two cases were identified; they were the result of a translocation of the SRY gene from the Y chromosome to the X chromosome during meiosis. An ultrasonographic difference may represent an otherwise unsuspected genetic abnormality.

Read the complete abstract on PubMed

Topics

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Share to Amniocentesis
Share to Gonadal Dysgenesis
Share to Pregnancy Trimester, Second

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

Share to Sex Chromosome Aberrations

Share to Sex-Determining Region Y Protein

Share to Translocation, Genetic

Share to Ultrasonography, Prenatal

Share to X Chromosome

Source

Identifiers

PMID: 10203670
DOI: 10.1016/s0002-9378(99)70673-3

Genes

SRY

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.

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Semantic proximity does not establish scientific evidence.

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Prenatal diagnosis of 46,XX male fetuses.PMID 10203670Read ↗

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Prenatal diagnosis of sex differentiation disorders: the role of fetal ultrasound.Semantic proximity Read ↗

Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.Semantic proximity Read ↗

Analysis of the SRY gene in a girl with 45,X/46,XY genotype.Semantic proximity Read ↗

Prenatal diagnosis of a 45,X male with a SRY-bearing chromosome 21.Semantic proximity Read ↗

Cell‐free fetal DNA sex determination identified a maternal SRY gene with a known X chromosome deletionSemantic proximity Read ↗

[XX male: 3 case reports during childhood].Semantic proximity Read ↗

Prenatal diagnosis of 46, XX male fetusSemantic proximity Read ↗

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