J. Horst

Frequencies of the most common mutations responsible for phenylketonuria in Poland.

C. Żekanowski, M. Nowacka, B. Cabalska, 1994, Molecular and cellular probes.

Clinical presentation and mutation identification in the NBS1 gene in a boy with Nijmegen breakage syndrome

M. Herrmann, B. Wittwer, A. Reis, 2000, Clinical genetics.

Factor VIII gene inversions in severe hemophilia A: results of an international consortium study.

F E Preston, P G Mori, S S Sommer, 1995, Blood.

Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells.

D. Schaid, P. Hutter, H. Kazazian, 1994, Human molecular genetics.

Human Y-chromosomal STR haplotypes in a Kurdish population sample

P. Forster, J. Horst, B. Brinkmann, 1999, International Journal of Legal Medicine.

Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndrome.

E. Obersztyn, D. Halley, T. Mazurczak, 1996, Acta biochimica Polonica.

Mutation Detection Rate in Female Patients with Reduced Factor VIII Activity and Negative Family History for Hemophilia A

H. Pollmann, U. Nowak‐Göttl, A. Todorova, 2008 .