Detalhe da pesquisa
1.
The Use of CGH Arrays for Identifying Copy Number Variations in Children with Autism Spectrum Disorder.
Brain Sci
; 14(3)2024 Mar 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38539661
2.
NGS analysis of collagen type I genes in Polish patients with Osteogenesis imperfecta: a nationwide multicenter study.
Front Endocrinol (Lausanne)
; 14: 1149982, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37810882
3.
Clinical characteristics of Polish patients with molecularly confirmed Mowat-Wilson syndrome.
J Appl Genet
; 62(3): 477-485, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33982229
4.
Exome Sequencing Reveals Novel Variants and Expands the Genetic Landscape for Congenital Microcephaly.
Genes (Basel)
; 12(12)2021 12 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34946966