APA
Hemati P., Revah-Politi A., Bassan H., Petrovski S., Bilancia C. G., Ramsey K., Griffin N. G., Bier L., Cho M. T., Rosello M., Lynch S. A., Colombo S., Weber A., Haug M., Heinzen E. L., Sands T. T., Narayanan V., Primiano M., Aggarwal V. S., Millan F., Sattler-Holtrop S. G., Caro-Llopis A., Pillar N., Baker J., Freedman R., Kroes H. Y., Sacharow S., Stong N., Lapunzina P., Schneider M. C., Mendelsohn N. J., Singleton A., Loik Ramey V., Wou K., Kuzminsky A., Monfort S., Weiss M., Doyle S., Iglesias A., Martinez F., Mckenzie F., Orellana C., van Gassen K. L. I., Palomares M., Bazak L., Lee A., Bircher A., Basel-Vanagaite L., Hafström M., Houge G., Goldstein D. B. & Anyane-Yeboa K. (20190925). Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature. : American journal of medical genetics. Part A.
Chicago
Hemati Parisa, Revah-Politi Anya, Bassan Haim, Petrovski Slavé, Bilancia Colleen G, Ramsey Keri, Griffin Nicole G, Bier Louise, Cho Megan T, Rosello Monica, Lynch Sally Ann, Colombo Sophie, Weber Astrid, Haug Marte, Heinzen Erin L, Sands Tristan T, Narayanan Vinodh, Primiano Michelle, Aggarwal Vimla S, Millan Francisca, Sattler-Holtrop Shannon G, Caro-Llopis Alfonso, Pillar Nir, Baker Janice, Freedman Rebecca, Kroes Hester Y, Sacharow Stephanie, Stong Nick, Lapunzina Pablo, Schneider Michael C, Mendelsohn Nancy J, Singleton Amanda, Loik Ramey Valerie, Wou Karen, Kuzminsky Alla, Monfort Sandra, Weiss Monica, Doyle Samantha, Iglesias Alejandro, Martinez Francisco, Mckenzie Fiona, Orellana Carmen, van Gassen Koen L I, Palomares Maria, Bazak Lily, Lee Andy, Bircher Ana, Basel-Vanagaite Lina, Hafström Maria, Houge Gunnar, Goldstein David B and Anyane-Yeboa Kwame. 20190925. Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature. : American journal of medical genetics. Part A.
Harvard
Hemati P., Revah-Politi A., Bassan H., Petrovski S., Bilancia C. G., Ramsey K., Griffin N. G., Bier L., Cho M. T., Rosello M., Lynch S. A., Colombo S., Weber A., Haug M., Heinzen E. L., Sands T. T., Narayanan V., Primiano M., Aggarwal V. S., Millan F., Sattler-Holtrop S. G., Caro-Llopis A., Pillar N., Baker J., Freedman R., Kroes H. Y., Sacharow S., Stong N., Lapunzina P., Schneider M. C., Mendelsohn N. J., Singleton A., Loik Ramey V., Wou K., Kuzminsky A., Monfort S., Weiss M., Doyle S., Iglesias A., Martinez F., Mckenzie F., Orellana C., van Gassen K. L. I., Palomares M., Bazak L., Lee A., Bircher A., Basel-Vanagaite L., Hafström M., Houge G., Goldstein D. B. and Anyane-Yeboa K. (20190925). Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature. : American journal of medical genetics. Part A.
MLA
Hemati Parisa, Revah-Politi Anya, Bassan Haim, Petrovski Slavé, Bilancia Colleen G, Ramsey Keri, Griffin Nicole G, Bier Louise, Cho Megan T, Rosello Monica, Lynch Sally Ann, Colombo Sophie, Weber Astrid, Haug Marte, Heinzen Erin L, Sands Tristan T, Narayanan Vinodh, Primiano Michelle, Aggarwal Vimla S, Millan Francisca, Sattler-Holtrop Shannon G, Caro-Llopis Alfonso, Pillar Nir, Baker Janice, Freedman Rebecca, Kroes Hester Y, Sacharow Stephanie, Stong Nick, Lapunzina Pablo, Schneider Michael C, Mendelsohn Nancy J, Singleton Amanda, Loik Ramey Valerie, Wou Karen, Kuzminsky Alla, Monfort Sandra, Weiss Monica, Doyle Samantha, Iglesias Alejandro, Martinez Francisco, Mckenzie Fiona, Orellana Carmen, van Gassen Koen L I, Palomares Maria, Bazak Lily, Lee Andy, Bircher Ana, Basel-Vanagaite Lina, Hafström Maria, Houge Gunnar, Goldstein David B and Anyane-Yeboa Kwame. Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature. : American journal of medical genetics. Part A. 20190925.