APA

Weksberg R., Teshima I., Williams B. R., Greenberg C. R., Pueschel S. M., Chernos J. E., Fowlow S. B., Hoyme E., Anderson I. J. & Whiteman D. A. (19930727). Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted. : Human molecular genetics.

Chicago

Weksberg R, Teshima I, Williams B R, Greenberg C R, Pueschel S M, Chernos J E, Fowlow S B, Hoyme E, Anderson I J and Whiteman D A. 19930727. Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted. : Human molecular genetics.

Harvard

Weksberg R., Teshima I., Williams B. R., Greenberg C. R., Pueschel S. M., Chernos J. E., Fowlow S. B., Hoyme E., Anderson I. J. and Whiteman D. A. (19930727). Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted. : Human molecular genetics.

MLA

Weksberg R, Teshima I, Williams B R, Greenberg C R, Pueschel S M, Chernos J E, Fowlow S B, Hoyme E, Anderson I J and Whiteman D A. Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted. : Human molecular genetics. 19930727.