Girisha, K. Et Al. 2022. Biallelic variants in KITLG cause Waardenburg syndrome type 2, albinism-deafness syndrome and oculocutaneous albinism. European Human Genetics Conference , (Vienna, Austria), 369.

Girisha, K., Vona, B., Schwartzbaum, D., Rodriguez, A. A., Lewis, S. S., Toosi, M. B., ... Radhakrishnan, P.(2022). Biallelic variants in KITLG cause Waardenburg syndrome type 2, albinism-deafness syndrome and oculocutaneous albinism . European Human Genetics Conference (pp.369). Vienna, Austria

Girisha, Katta Et Al. "Biallelic variants in KITLG cause Waardenburg syndrome type 2, albinism-deafness syndrome and oculocutaneous albinism," European Human Genetics Conference , Vienna, Austria, 2022

Girisha, Katta Et Al. "Biallelic variants in KITLG cause Waardenburg syndrome type 2, albinism-deafness syndrome and oculocutaneous albinism." European Human Genetics Conference , Vienna, Austria, pp.369, 2022

Girisha, K. Et Al. (2022) . "Biallelic variants in KITLG cause Waardenburg syndrome type 2, albinism-deafness syndrome and oculocutaneous albinism." European Human Genetics Conference , Vienna, Austria, p.369.

@conferencepaper{conferencepaper, author={Katta Girisha Et Al. }, title={Biallelic variants in KITLG cause Waardenburg syndrome type 2, albinism-deafness syndrome and oculocutaneous albinism}, congress name={European Human Genetics Conference }, city={Vienna}, country={Austria}, year={2022}, pages={369} }