Cerosaletti, K. M., Lange, E., Stringham, H. M., Weemaes, C. M., Smeets, D., Sölder, B., . . . Concannon, P. (1998). Fine localization of the Nijmegen breakage syndrome gene to 8q21: Evidence for a common founder haplotype.
শিকাগো স্টাইলে সাইটেশনCerosaletti, K M., et al. Fine Localization of the Nijmegen Breakage Syndrome Gene to 8q21: Evidence for a Common Founder Haplotype. 1998.
এমএলএ সাইটেশনCerosaletti, K M., et al. Fine Localization of the Nijmegen Breakage Syndrome Gene to 8q21: Evidence for a Common Founder Haplotype. 1998.
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