APA
Jaureguiberry G., De la Dure-Molla M., Parry D., Quentric M., Himmerkus N., Koike T., Poulter J., Klootwijk E., Robinette S. L., Howie A. J., Patel V., Figueres M., Stanescu H. C., Issler N., Nicholson J. K., Bockenhauer D., Laing C., Walsh S. B., McCredie D. A., Povey S., Asselin A., Picard A., Coulomb A., Medlar A. J., Bailleul-Forestier I., Verloes A., Le Caignec C., Roussey G., Guiol J., Isidor B., Logan C., Shore R., Johnson C., Inglehearn C., Al-Bahlani S., Schmittbuhl M., Clauss F., Huckert M., Laugel V., Ginglinger E., Pajarola S., Spartà G., Bartholdi D., Rauch A., Addor M., Yamaguti P. M., Safatle H. P., Acevedo A. C., Martelli-Júnior H., dos Santos Netos P. E., Coletta R. D., Gruessel S., Sandmann C., Ruehmann D., Langman C. B., Scheinman S. J., Ozdemir-Ozenen D., Hart T. C., Hart P. S., Neugebauer U., Schlatter E., Houillier P., Gahl W. A., Vikkula M., Bloch-Zupan A., Bleich M., Kitagawa H., Unwin R. J., Mighell A., Berdal A. & Kleta R. (20131025). Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations. : Nephron. Physiology.
Chicago
Jaureguiberry Graciana, De la Dure-Molla Muriel, Parry David, Quentric Mickael, Himmerkus Nina, Koike Toshiyasu, Poulter James, Klootwijk Enriko, Robinette Steven L, Howie Alexander J, Patel Vaksha, Figueres Marie-Lucile, Stanescu Horia C, Issler Naomi, Nicholson Jeremy K, Bockenhauer Detlef, Laing Christopher, Walsh Stephen B, McCredie David A, Povey Sue, Asselin Audrey, Picard Arnaud, Coulomb Aurore, Medlar Alan J, Bailleul-Forestier Isabelle, Verloes Alain, Le Caignec Cedric, Roussey Gwenaelle, Guiol Julien, Isidor Bertrand, Logan Clare, Shore Roger, Johnson Colin, Inglehearn Christopher, Al-Bahlani Suhaila, Schmittbuhl Matthieu, Clauss François, Huckert Mathilde, Laugel Virginie, Ginglinger Emmanuelle, Pajarola Sandra, Spartà Giuseppina, Bartholdi Deborah, Rauch Anita, Addor Marie-Claude, Yamaguti Paulo M, Safatle Heloisa P, Acevedo Ana Carolina, Martelli-Júnior Hercílio, dos Santos Netos Pedro E, Coletta Ricardo D, Gruessel Sandra, Sandmann Carolin, Ruehmann Denise, Langman Craig B, Scheinman Steven J, Ozdemir-Ozenen Didem, Hart Thomas C, Hart P Suzanne, Neugebauer Ute, Schlatter Eberhard, Houillier Pascal, Gahl William A, Vikkula Miikka, Bloch-Zupan Agnès, Bleich Markus, Kitagawa Hiroshi, Unwin Robert J, Mighell Alan, Berdal Ariane and Kleta Robert. 20131025. Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations. : Nephron. Physiology.
Harvard
Jaureguiberry G., De la Dure-Molla M., Parry D., Quentric M., Himmerkus N., Koike T., Poulter J., Klootwijk E., Robinette S. L., Howie A. J., Patel V., Figueres M., Stanescu H. C., Issler N., Nicholson J. K., Bockenhauer D., Laing C., Walsh S. B., McCredie D. A., Povey S., Asselin A., Picard A., Coulomb A., Medlar A. J., Bailleul-Forestier I., Verloes A., Le Caignec C., Roussey G., Guiol J., Isidor B., Logan C., Shore R., Johnson C., Inglehearn C., Al-Bahlani S., Schmittbuhl M., Clauss F., Huckert M., Laugel V., Ginglinger E., Pajarola S., Spartà G., Bartholdi D., Rauch A., Addor M., Yamaguti P. M., Safatle H. P., Acevedo A. C., Martelli-Júnior H., dos Santos Netos P. E., Coletta R. D., Gruessel S., Sandmann C., Ruehmann D., Langman C. B., Scheinman S. J., Ozdemir-Ozenen D., Hart T. C., Hart P. S., Neugebauer U., Schlatter E., Houillier P., Gahl W. A., Vikkula M., Bloch-Zupan A., Bleich M., Kitagawa H., Unwin R. J., Mighell A., Berdal A. and Kleta R. (20131025). Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations. : Nephron. Physiology.
MLA
Jaureguiberry Graciana, De la Dure-Molla Muriel, Parry David, Quentric Mickael, Himmerkus Nina, Koike Toshiyasu, Poulter James, Klootwijk Enriko, Robinette Steven L, Howie Alexander J, Patel Vaksha, Figueres Marie-Lucile, Stanescu Horia C, Issler Naomi, Nicholson Jeremy K, Bockenhauer Detlef, Laing Christopher, Walsh Stephen B, McCredie David A, Povey Sue, Asselin Audrey, Picard Arnaud, Coulomb Aurore, Medlar Alan J, Bailleul-Forestier Isabelle, Verloes Alain, Le Caignec Cedric, Roussey Gwenaelle, Guiol Julien, Isidor Bertrand, Logan Clare, Shore Roger, Johnson Colin, Inglehearn Christopher, Al-Bahlani Suhaila, Schmittbuhl Matthieu, Clauss François, Huckert Mathilde, Laugel Virginie, Ginglinger Emmanuelle, Pajarola Sandra, Spartà Giuseppina, Bartholdi Deborah, Rauch Anita, Addor Marie-Claude, Yamaguti Paulo M, Safatle Heloisa P, Acevedo Ana Carolina, Martelli-Júnior Hercílio, dos Santos Netos Pedro E, Coletta Ricardo D, Gruessel Sandra, Sandmann Carolin, Ruehmann Denise, Langman Craig B, Scheinman Steven J, Ozdemir-Ozenen Didem, Hart Thomas C, Hart P Suzanne, Neugebauer Ute, Schlatter Eberhard, Houillier Pascal, Gahl William A, Vikkula Miikka, Bloch-Zupan Agnès, Bleich Markus, Kitagawa Hiroshi, Unwin Robert J, Mighell Alan, Berdal Ariane and Kleta Robert. Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations. : Nephron. Physiology. 20131025.