Sandal, S. Et Al. 2024. A 37-kb Deletion in Region 16p13.3 in an Infant with Osteopetrosis and Congenital Diarrhea Including the CLCN7 and PERCC1 Genes. MOLECULAR SYNDROMOLOGY , vol.15, no.5 , 427-431.

Sandal, S., KAYHAN, G., Kahvecioglu, D., Vezir, E., Kilic, A., Kose, A., ... Ersun, M. T.(2024). A 37-kb Deletion in Region 16p13.3 in an Infant with Osteopetrosis and Congenital Diarrhea Including the CLCN7 and PERCC1 Genes. MOLECULAR SYNDROMOLOGY , vol.15, no.5, 427-431.

Sandal, Semih Et Al. "A 37-kb Deletion in Region 16p13.3 in an Infant with Osteopetrosis and Congenital Diarrhea Including the CLCN7 and PERCC1 Genes," MOLECULAR SYNDROMOLOGY , vol.15, no.5, 427-431, 2024

Sandal, Semih Et Al. "A 37-kb Deletion in Region 16p13.3 in an Infant with Osteopetrosis and Congenital Diarrhea Including the CLCN7 and PERCC1 Genes." MOLECULAR SYNDROMOLOGY , vol.15, no.5, pp.427-431, 2024

Sandal, S. Et Al. (2024) . "A 37-kb Deletion in Region 16p13.3 in an Infant with Osteopetrosis and Congenital Diarrhea Including the CLCN7 and PERCC1 Genes." MOLECULAR SYNDROMOLOGY , vol.15, no.5, pp.427-431.

@article{article, author={Semih Sandal Et Al. }, title={A 37-kb Deletion in Region 16p13.3 in an Infant with Osteopetrosis and Congenital Diarrhea Including the CLCN7 and PERCC1 Genes}, journal={MOLECULAR SYNDROMOLOGY}, year=2024, pages={427-431} }