APA

Archer H. L., Evans J. C., Millar D. S., Thompson P. W., Kerr A. M., Leonard H., Christodoulou J., Ravine D., Lazarou L., Grove L., Verity C., Whatley S. D., Pilz D. T., Sampson J. R. & Clarke A. J. (20060530). NTNG1 mutations are a rare cause of Rett syndrome. : American journal of medical genetics. Part A.

Chicago

Archer Hayley L, Evans Julie C, Millar David S, Thompson Peter W, Kerr Alison M, Leonard Helen, Christodoulou John, Ravine David, Lazarou Lazarus, Grove Lucy, Verity Christopher, Whatley Sharon D, Pilz Daniela T, Sampson Julian R and Clarke Angus J. 20060530. NTNG1 mutations are a rare cause of Rett syndrome. : American journal of medical genetics. Part A.

Harvard

Archer H. L., Evans J. C., Millar D. S., Thompson P. W., Kerr A. M., Leonard H., Christodoulou J., Ravine D., Lazarou L., Grove L., Verity C., Whatley S. D., Pilz D. T., Sampson J. R. and Clarke A. J. (20060530). NTNG1 mutations are a rare cause of Rett syndrome. : American journal of medical genetics. Part A.

MLA

Archer Hayley L, Evans Julie C, Millar David S, Thompson Peter W, Kerr Alison M, Leonard Helen, Christodoulou John, Ravine David, Lazarou Lazarus, Grove Lucy, Verity Christopher, Whatley Sharon D, Pilz Daniela T, Sampson Julian R and Clarke Angus J. NTNG1 mutations are a rare cause of Rett syndrome. : American journal of medical genetics. Part A. 20060530.