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Ahmad, I., Baig, S. M., Abdulkareem, A. R., Hussain, M. S., Sur, I., Toliat, M. R., Nuernberg, G., Dalibor, N., Moawia, A., Waseem, S. S., Asif, M., Nagra, H., Sher, M., Khan, M. M. A., Hassan, I., Rehman, S. Ur, Thiele, H., Altmueller, J., Noegel, A. A. and Nuernberg, P. (2017). Genetic heterogeneity in Pakistani microcephaly families revisited. Clin. Genet., 92 (1). S. 62 - 69. HOBOKEN: WILEY. ISSN 1399-0004
Farooq, M., Lindbaek, L., Krogh, N., Nielsen, V. S., Monnich, M., Sakthivel, S., Doganli, C., Mang, Y., Fatima, A., Hussain, M. S., Mollgard, K., Eiberg, H., Hansen, L., Kjaer, K. W., Nielsen, H., Baig, S. M., Tommerup, N., Christensen, S. T. and Larsen, L. A. (2018). Mutation of ribosomal RNA-processing protein 7 homolog A (RRP7A) cause autosomal recessive microcephaly with intellectual disability. Eur. J. Hum. Genet., 26. S. 112 - 113. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438
Iqbal, M., Baig, S. M., Abdullah, U., Makhdoom, E. U. H., Ali, Z., Khan, S., Jameel, M., Noegel, A. A., Nuernberg, P., Osmond, M. and Hussain, M. S. (2020). Mutations of PCDHGC4 encoding protocadherin gamma-C4 cause primary microcephaly and intellectual disability. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 399 - 401. LONDON: SPRINGERNATURE. ISSN 1476-5438