APA

Roche E. F., McGowan A., Koulouri O., Turgeon M., Nicholas A. K., Heffernan E., El-Khairi R., Abid N., Lyons G., Halsall D., Bonomi M., Persani L., Dattani M. T., Gurnell M., Bernard D. J. & Schoenmakers N. (20191202). A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome. : Clinical endocrinology.

Chicago

Roche Edna F, McGowan Anne, Koulouri Olympia, Turgeon Marc-Olivier, Nicholas Adeline K, Heffernan Emmeline, El-Khairi Ranna, Abid Noina, Lyons Greta, Halsall David, Bonomi Marco, Persani Luca, Dattani Mehul T, Gurnell Mark, Bernard Daniel J and Schoenmakers Nadia. 20191202. A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome. : Clinical endocrinology.

Harvard

Roche E. F., McGowan A., Koulouri O., Turgeon M., Nicholas A. K., Heffernan E., El-Khairi R., Abid N., Lyons G., Halsall D., Bonomi M., Persani L., Dattani M. T., Gurnell M., Bernard D. J. and Schoenmakers N. (20191202). A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome. : Clinical endocrinology.

MLA

Roche Edna F, McGowan Anne, Koulouri Olympia, Turgeon Marc-Olivier, Nicholas Adeline K, Heffernan Emmeline, El-Khairi Ranna, Abid Noina, Lyons Greta, Halsall David, Bonomi Marco, Persani Luca, Dattani Mehul T, Gurnell Mark, Bernard Daniel J and Schoenmakers Nadia. A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome. : Clinical endocrinology. 20191202.