Petersen MB. Mini review. Non-syndromic autosomal-dominant deafness. Clin Genet 2002;62:1-13.
Petersen MB, Willems PJ. Review. Non-syndromic, autosomal-recessive deafness. Clin Genet 2006;69:371-392. (pdf)
Kokotas H, Petersen MB, Willems PJ. Mitochondrial deafness. Clin Genet 2007;71:379-391. (pdf)
Petersen MB, Wang Q, Willems PJ. Sex-linked deafness. Clin Genet 2008;73:14-23. (pdf)
Kokotas H, Grigoriadou M, Petersen MB. Meiotic nondisjunction - the major cause of trisomy 21. In: Egel R & Lankenau D-H (eds): Recombination and Meiosis – Crossing-Over and Disjunction, Springer-Verlag, Berlin Heidelberg 2008;245-278. (pdf)
|
