Clinical and Genetic Aspects of Verheij Syndrome in Two Cases

A very rare syndrome - Verheij syndrome - is reported in 2 cases with genotype phenotype correlation in this report.

Authors

Hakan Gürkan (ORCID: https://orcid.org/0000-0002-8967-6124)
Hazal Sezginer Guler
Drenushe Zhuri̇ (ORCID: https://orcid.org/0000-0002-8370-1990)
Sinem Yalçıntepe (ORCID: https://orcid.org/0000-0002-8557-8885)
Yade Dilay Kursat

Institutions

Trakya University (TR)

Publication Details

Journal: Molecular Syndromology
Published: 2025-03-25
DOI: https://doi.org/10.1159/000545448
Primary Topic: Genomic variations and chromosomal abnormalities
Type: article
Field-Weighted Citation Impact: 0.00

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article

Clinical and Genetic Aspects of Verheij Syndrome in Two Cases

Hakan Gürkan, Hazal Sezginer Guler, Drenushe Zhuri̇, Sinem Yalçıntepe et al.

Mar 25, 2025

Molecular Syndromology

Genomic variations and chromosomal abnormalities

article

Clinical and Genetic Aspects of Verheij Syndrome in Two Cases

Hakan Gürkan, Hazal Sezginer Guler, Drenushe Zhuri̇, Sinem Yalçıntepe, Yade Dilay Kursat

March 25, 2025article en

Abstract

A very rare syndrome - Verheij syndrome - is reported in 2 cases with genotype phenotype correlation in this report.

Molecular SyndromologyVol. 17(1)

Trakya University (TR)

Openalex Percentile: Top 93%

Genomic variations and chromosomal abnormalities

DOI Open Access PDF OpenAlex

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Clinical and Genetic Aspects of Verheij Syndrome in Two Cases — Hakan Gürkan, Hazal Sezginer Guler, et al. · Molecular Syndromology (2025) | TGRS Research Map | TGRS