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Identification of gene variants in a cohort of hypogonadotropic hypogonadism: Diagnostic utility of custom NGS panel and WES in unravelling genetic complexity of the disease.
Mol Cell Endocrinol. 2020 Nov 1;517:110968. doi: 10.1016/j.mce.2020.110968. Epub 2020 Aug 4.
Mol Cell Endocrinol. 2020.
PMID: 32763379
The Use of CGH Arrays for Identifying Copy Number Variations in Children with Autism Spectrum Disorder.
Kucińska A, Hawuła W, Rutkowska L, Wysocka U, Kępczyński Ł, Piotrowicz M, Chilarska T, Wieczorek-Cichecka N, Połatyńska K, Przysło Ł, Gach A.
Kucińska A, et al.
Brain Sci. 2024 Mar 13;14(3):273. doi: 10.3390/brainsci14030273.
Brain Sci. 2024.
PMID: 38539661
Free PMC article.
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