S. Mercan Et Al. , "Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity.," Genes & genomics , vol.45, no.1, pp.13-21, 2023
Mercan, S. Et Al. 2023. Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity.. Genes & genomics , vol.45, no.1 , 13-21.
Mercan, S., Akcakaya, N. H., Salman, B., Yapici, Z., Ozbek, U., & Ugur Iseri, S. A., (2023). Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity.. Genes & genomics , vol.45, no.1, 13-21.
Mercan, Sevcan Et Al. "Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity.," Genes & genomics , vol.45, no.1, 13-21, 2023
Mercan, Sevcan Et Al. "Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity.." Genes & genomics , vol.45, no.1, pp.13-21, 2023
Mercan, S. Et Al. (2023) . "Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity.." Genes & genomics , vol.45, no.1, pp.13-21.
@article{article, author={Sevcan Mercan Et Al. }, title={Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity.}, journal={Genes & genomics}, year=2023, pages={13-21} }