Placental Teratoma Presenting as a Lobulated Mass behind the Neck of Fetus: A Case Report

por Prashanth, Adiga, Lavanya, Rai, Girisha, K. M., Mundkur, Anjali
Publicado 2012

Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss

por Vona, B., Schwartzbaum, D.A., Rodriguez, A.A., Lewis, S.S., Toosi, M.B., Radhakrishnan, P., Bozan, N., Akın, R., Doosti, M., Manju, R., Duman, D., Sineni, C.J., Nampoothiri, S., Karimiani, E.G., Houlden, H., Bademci, G., Tekin, M., Girisha, K.M., Maroofian, R., Douzgou, S.
Publicado 2022

Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies

por Hammarsjö, A., Wang, Z., Vaz, R., Taylan, F., Sedghi, M., Girisha, K. M., Chitayat, D., Neethukrishna, K., Shannon, P., Godoy, R., Gowrishankar, K., Lindstrand, A., Nasiri, J., Baktashian, M., Newton, P. T., Guo, L., Hofmeister, W., Pettersson, M., Chagin, A. S., Nishimura, G., Yan, L., Matsumoto, N., Nordgren, A., Miyake, N., Grigelioniene, G., Ikegawa, S.
Publicado 2017