Wanda Hawula
281/289 Rzgowska St
Lodz, LD, Poland
Lodz, LD, Poland
Last Updated: 09/26/2026
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Found 11 publications
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: March 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: March 27, 2026
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
Broad phenotypic spectrum of germ line 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia.
Journal: Genes, chromosomes & cancer
Published: July 12, 2020
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
Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome.
Journal: American journal of human genetics
Published: September 04, 2015
The association between environmental exposure to pyrethroids and sperm aneuploidy.
Journal: Chemosphere
Published: March 07, 2014
Human sperm aneuploidy after exposure to polycyclic aromatic hydrocarbons.
Journal: Reproduction, fertility, and development
Published: February 17, 2014
Human urinary phthalate metabolites level and main semen parameters, sperm chromatin structure, sperm aneuploidy and reproductive hormones.
Journal: Reproductive toxicology (Elmsford, N.Y.)
Published: December 05, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026