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Article

Prenatal diagnosis of Apert syndrome.

Fetal diagnosis and therapy - 1 Jan 2000

Hansen Wendy F, Rijhsinghani Asha, Grant Stanley, Yankowitz Jerome

Abstract excerpt

OBJECTIVE: The role of the human fibroblast growth factor receptor (FGFR) gene family in current prenatal diagnosis and management of craniosynostosis syndromes and skeletal dysplasias is discussed. METHOD: We present the antenatal ultrasound findings, diagnosis, and management of 2 cases of Aper...

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Source

Identifiers

PMID: 14764955
DOI: 10.1159/000075135

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14764955-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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