APA

Poulter J. A., El-Sayed W., Shore R. C., Kirkham J., Inglehearn C. F. & Mighell A. J. (20150212). Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta. : European journal of human genetics : EJHG.

Chicago

Poulter James A, El-Sayed Walid, Shore Roger C, Kirkham Jennifer, Inglehearn Chris F and Mighell Alan J. 20150212. Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta. : European journal of human genetics : EJHG.

Harvard

Poulter J. A., El-Sayed W., Shore R. C., Kirkham J., Inglehearn C. F. and Mighell A. J. (20150212). Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta. : European journal of human genetics : EJHG.

MLA

Poulter James A, El-Sayed Walid, Shore Roger C, Kirkham Jennifer, Inglehearn Chris F and Mighell Alan J. Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta. : European journal of human genetics : EJHG. 20150212.