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pro vyhledávání: '"Calin Lazar"'
Autor:
Alexandru Cristian Bolunduț, Florina Nazarie, Cecilia Lazea, Crina Șufană, Diana Miclea, Călin Lazăr, Carmen Mihaela Mihu
Publikováno v:
Genes, Vol 15, Iss 2, p 207 (2024)
Congenital heart defects (CHDs) have had an increasing prevalence over the last decades, being one of the most common congenital defects. Their etiopathogenesis is multifactorial in origin. About 10–15% of all CHD can be attributed to copy number v
Externí odkaz:
https://doaj.org/article/c5fe28cc7bd145b09c4d157b361513ba
Autor:
Anca-Lelia Riza, Camelia Alkhzouz, Marius Farcaș, Andrei Pîrvu, Diana Miclea, Gheorghe Mihuț, Răzvan-Mihail Pleșea, Delia Ștefan, Mihaela Drodar, Călin Lazăr, on behalf of the HINT Study, on behalf of the FUSE Study, Mihai Ioana, Radu Popp
Publikováno v:
Genes, Vol 14, Iss 1, p 69 (2022)
The genetic causes of autosomal recessive nonsyndromic hearing loss (ARNSHL) are heterogeneous and highly ethnic-specific. We describe GJB2 (connexin 26) variants and carrier frequencies as part of our study and summarize previously reported ones for
Externí odkaz:
https://doaj.org/article/dc8118aa06e442daab7f1e9d7d3d206f