Zsuzsanna Szucs

University of Debrecen

Hungary

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Articles (8)

Double Heterozygosity for Rare Deleterious Variants in the BRCA1 and BRCA2 Genes in a Hungarian Patient with Breast Cancer

Year:

2023

Establishing the Mutational Spectrum of Hungarian Patients with Familial Hypercholesterolemia

Year:

2022

Helsmoortel–Van der Aa Syndrome—Cardiothoracic and Ectodermal Manifestations in Two Patients as Further Support of a Previous Observation on Phenotypic Overlap with RASopathies

Year:

2022

An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient

Year:

2022

Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review

Year:

2021

Four New Cases of Hypomyelinating Leukodystrophy Associated with the UFM1 c.-155_-153delTCA Founder Mutation in Pediatric Patients of Roma Descent in Hungary

Year:

2021

A Comprehensive Analysis of Hungarian MODY Patients—Part II: Glucokinase MODY Is the Most Prevalent Subtype Responsible for about 70% of Confirmed Cases

Year:

2021

A Comprehensive Analysis of Hungarian MODY Patients—Part I: Gene Panel Sequencing Reveals Pathogenic Mutations in HNF1A, HNF1B, HNF4A, ABCC8 and INS Genes

Year:

2021

Collaborators (3)

Mariann Harangi

Associate professor

University of Debrecen Medical School and Health Science Center

HUNGARY

Endre Barta

University of Debrecen

HUNGARY

Istvan Balogh

Head

University of Debrecen

HUNGARY

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