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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

This list was generated on Thu May 9 01:06:01 2024 CEST.