Novel Missense Variant in the <i>FGFR1</i> Gene Associated With Prenatal Diagnosis of Hartsfield Syndrome

Authors

Madeline Dyke (ORCID: https://orcid.org/0009-0008-6504-3278)
Morrison Hodges (ORCID: https://orcid.org/0009-0004-0499-1427)
Kelly L. Gilmore (ORCID: https://orcid.org/0000-0002-9125-8714)
Neeta L. Vora

Institutions

University of North Carolina at Chapel Hill (US)

Publication Details

Journal: Prenatal Diagnosis
Published: 2025-11-14
DOI: https://doi.org/10.1002/pd.70019
Primary Topic: Hedgehog Signaling Pathway Studies
Type: article
Field-Weighted Citation Impact: 0.00

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article

Novel Missense Variant in the FGFR1 Gene Associated With Prenatal Diagnosis of Hartsfield Syndrome

Madeline Dyke, Morrison Hodges, Kelly L. Gilmore, Neeta L. Vora

Nov 14, 2025

Prenatal Diagnosis

Hedgehog Signaling Pathway Studies

article

Novel Missense Variant in the FGFR1 Gene Associated With Prenatal Diagnosis of Hartsfield Syndrome

Madeline Dyke, Morrison Hodges, Kelly L. Gilmore, Neeta L. Vora

November 14, 2025article en

Abstract

No abstract available for this paper.

Prenatal DiagnosisVol. 45(13)

University of North Carolina at Chapel Hill (US)

Openalex Percentile: Top 69%

Hedgehog Signaling Pathway Studies

DOI Source OpenAlex

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Novel Missense Variant in the <i>FGFR1</i> Gene Associated With Prenatal Diagnosis of Hartsfield Syndrome — Madeline Dyke, Morrison Hodges, et al. · Prenatal Diagnosis (2025) | TGRS Research Map | TGRS