APA

Schuster B., Knies K., Stoepker C., Velleuer E., Friedl R., Gottwald-Mühlhauser B., de Winter J. P. & Schindler D. (20130701). Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX4/FANCP. : Human mutation.

Chicago

Schuster Beatrice, Knies Kerstin, Stoepker Chantal, Velleuer Eunike, Friedl Richard, Gottwald-Mühlhauser Birgit, de Winter Johan P and Schindler Detlev. 20130701. Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX4/FANCP. : Human mutation.

Harvard

Schuster B., Knies K., Stoepker C., Velleuer E., Friedl R., Gottwald-Mühlhauser B., de Winter J. P. and Schindler D. (20130701). Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX4/FANCP. : Human mutation.

MLA

Schuster Beatrice, Knies Kerstin, Stoepker Chantal, Velleuer Eunike, Friedl Richard, Gottwald-Mühlhauser Birgit, de Winter Johan P and Schindler Detlev. Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX4/FANCP. : Human mutation. 20130701.