APA

Bartholdi D., Krajewska-Walasek M., Ounap K., Gaspar H., Chrzanowska K. H., Ilyana H., Kayserili H., Lurie I. W., Schinzel A. & Baumer A. (20090521). Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes. : Journal of medical genetics.

Chicago

Bartholdi D, Krajewska-Walasek M, Ounap K, Gaspar H, Chrzanowska K H, Ilyana H, Kayserili H, Lurie I W, Schinzel A and Baumer A. 20090521. Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes. : Journal of medical genetics.

Harvard

Bartholdi D., Krajewska-Walasek M., Ounap K., Gaspar H., Chrzanowska K. H., Ilyana H., Kayserili H., Lurie I. W., Schinzel A. and Baumer A. (20090521). Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes. : Journal of medical genetics.

MLA

Bartholdi D, Krajewska-Walasek M, Ounap K, Gaspar H, Chrzanowska K H, Ilyana H, Kayserili H, Lurie I W, Schinzel A and Baumer A. Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes. : Journal of medical genetics. 20090521.