Malgorzata Piotrowicz
Lodz, LD 93338, Poland
Last Updated: 09/26/2026
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Found 11 publications
Expanding the Molecular Landscape of Androgen Insensitivity Syndrome Through Next-Generation Sequencing.
Journal: The application of clinical genetics
Published: September 27, 2024
Correction: Kucińska et al. The Use of CGH Arrays for Identifying Copy Number Variations in Children with Autism Spectrum Disorder. Brain Sci. 2024, 14, 273.
Journal: Brain sciences
Published: April 07, 2024
NGS analysis of collagen type I genes in Polish patients with Osteogenesis imperfecta: a nationwide multicenter study.
Journal: Frontiers in endocrinology
Published: January 23, 2023
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome.
Journal: Genes
Published: November 19, 2022
Immune Dysregulation in Patients With Chromosome 18q Deletions-Searching for Putative Loci for Autoimmunity and Immunodeficiency.
Journal: Frontiers in immunology
Published: July 16, 2021
Comprehensive genomic analysis of patients with disorders of cerebral cortical development.
Journal: European journal of human genetics : EJHG
Published: April 10, 2017
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.
Journal: Circulation. Cardiovascular genetics
Published: December 16, 2016
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome.
Journal: Human genetics
Published: October 16, 2015
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.
Journal: American journal of human genetics
Published: December 04, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026