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 and 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 and Genomics , vol.45, no.1 , 13-21.
Mercan, S., Akcakaya, N. H., Salman, B., Yapici, Z., ÖZBEK, U., & UĞUR İŞERİ, 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 and 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 and 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 and 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 and 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 and Genomics}, year=2023, pages={13-21} }