APA

Casey J. P., Magalhaes T., Conroy J. M., Regan R., Shah N., Anney R., Shields D. C., Abrahams B. S., Almeida J., Bacchelli E., Bailey A. J., Baird G., Battaglia A., Berney T., Bolshakova N., Bolton P. F., Bourgeron T., Brennan S., Cali P., Correia C., Corsello C., Coutanche M., Dawson G., de Jonge M., Delorme R., Duketis E., Duque F., Estes A., Farrar P., Fernandez B. A., Folstein S. E., Foley S., Fombonne E., Freitag C. M., Gilbert J., Gillberg C., Glessner J. T., Green J., Guter S. J., Hakonarson H., Holt R., Hughes G., Hus V., Igliozzi R., Kim C., Klauck S. M., Kolevzon A., Lamb J. A., Leboyer M., Le Couteur A., Leventhal B. L., Lord C., Lund S. C., Maestrini E., Mantoulan C., Marshall C. R., McConachie H., McDougle C. J., McGrath J., McMahon W. M., Merikangas A., Miller J., Minopoli F., Mirza G. K., Munson J., Nelson S. F., Nygren G., Oliveira G., Pagnamenta A. T., Papanikolaou K., Parr J. R., Parrini B., Pickles A., Pinto D., Piven J., Posey D. J., Poustka A., Poustka F., Ragoussis J., Roge B., Rutter M. L., Sequeira A. F., Soorya L., Sousa I., Sykes N., Stoppioni V., Tancredi R., Tauber M., Thompson A. P., Thomson S., Tsiantis J., Van Engeland H., Vincent J. B., Volkmar F., Vorstman J. A. S., Wallace S., Wang K., Wassink T. H., White K., Wing K., Wittemeyer K., Yaspan B. L., Zwaigenbaum L., Betancur C., Buxbaum J. D., Cantor R. M., Cook E. H., Coon H., Cuccaro M. L., Geschwind D. H., Haines J. L., Hallmayer J., Monaco A. P., Nurnberger J. I., Pericak-Vance M. A., Schellenberg G. D., Scherer S. W., Sutcliffe J. S., Szatmari P., Vieland V. J., Wijsman E. M., Green A., Gill M., Gallagher L., Vicente A. & Ennis S. (20120514). A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. : Human genetics.

Chicago

Casey Jillian P, Magalhaes Tiago, Conroy Judith M, Regan Regina, Shah Naisha, Anney Richard, Shields Denis C, Abrahams Brett S, Almeida Joana, Bacchelli Elena, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Cali Phil, Correia Catarina, Corsello Christina, Coutanche Marc, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Foley Suzanne, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Holt Richard, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Lamb Janine A, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lord Catherine, Lund Sabata C, Maestrini Elena, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Merikangas Alison, Miller Judith, Minopoli Fiorella, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Nygren Gudrun, Oliveira Guiomar, Pagnamenta Alistair T, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Pickles Andrew, Pinto Dalila, Piven Joseph, Posey David J, Poustka Annemarie, Poustka Fritz, Ragoussis Jiannis, Roge Bernadette, Rutter Michael L, Sequeira Ana F, Soorya Latha, Sousa Inês, Sykes Nuala, Stoppioni Vera, Tancredi Raffaella, Tauber Maïté, Thompson Ann P, Thomson Susanne, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Vorstman Jacob A S, Wallace Simon, Wang Kai, Wassink Thomas H, White Kathy, Wing Kirsty, Wittemeyer Kerstin, Yaspan Brian L, Zwaigenbaum Lonnie, Betancur Catalina, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Geschwind Daniel H, Haines Jonathan L, Hallmayer Joachim, Monaco Anthony P, Nurnberger John I, Pericak-Vance Margaret A, Schellenberg Gerard D, Scherer Stephen W, Sutcliffe James S, Szatmari Peter, Vieland Veronica J, Wijsman Ellen M, Green Andrew, Gill Michael, Gallagher Louise, Vicente Astrid and Ennis Sean. 20120514. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. : Human genetics.

Harvard

Casey J. P., Magalhaes T., Conroy J. M., Regan R., Shah N., Anney R., Shields D. C., Abrahams B. S., Almeida J., Bacchelli E., Bailey A. J., Baird G., Battaglia A., Berney T., Bolshakova N., Bolton P. F., Bourgeron T., Brennan S., Cali P., Correia C., Corsello C., Coutanche M., Dawson G., de Jonge M., Delorme R., Duketis E., Duque F., Estes A., Farrar P., Fernandez B. A., Folstein S. E., Foley S., Fombonne E., Freitag C. M., Gilbert J., Gillberg C., Glessner J. T., Green J., Guter S. J., Hakonarson H., Holt R., Hughes G., Hus V., Igliozzi R., Kim C., Klauck S. M., Kolevzon A., Lamb J. A., Leboyer M., Le Couteur A., Leventhal B. L., Lord C., Lund S. C., Maestrini E., Mantoulan C., Marshall C. R., McConachie H., McDougle C. J., McGrath J., McMahon W. M., Merikangas A., Miller J., Minopoli F., Mirza G. K., Munson J., Nelson S. F., Nygren G., Oliveira G., Pagnamenta A. T., Papanikolaou K., Parr J. R., Parrini B., Pickles A., Pinto D., Piven J., Posey D. J., Poustka A., Poustka F., Ragoussis J., Roge B., Rutter M. L., Sequeira A. F., Soorya L., Sousa I., Sykes N., Stoppioni V., Tancredi R., Tauber M., Thompson A. P., Thomson S., Tsiantis J., Van Engeland H., Vincent J. B., Volkmar F., Vorstman J. A. S., Wallace S., Wang K., Wassink T. H., White K., Wing K., Wittemeyer K., Yaspan B. L., Zwaigenbaum L., Betancur C., Buxbaum J. D., Cantor R. M., Cook E. H., Coon H., Cuccaro M. L., Geschwind D. H., Haines J. L., Hallmayer J., Monaco A. P., Nurnberger J. I., Pericak-Vance M. A., Schellenberg G. D., Scherer S. W., Sutcliffe J. S., Szatmari P., Vieland V. J., Wijsman E. M., Green A., Gill M., Gallagher L., Vicente A. and Ennis S. (20120514). A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. : Human genetics.

MLA

Casey Jillian P, Magalhaes Tiago, Conroy Judith M, Regan Regina, Shah Naisha, Anney Richard, Shields Denis C, Abrahams Brett S, Almeida Joana, Bacchelli Elena, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Cali Phil, Correia Catarina, Corsello Christina, Coutanche Marc, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Foley Suzanne, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Holt Richard, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Lamb Janine A, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lord Catherine, Lund Sabata C, Maestrini Elena, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Merikangas Alison, Miller Judith, Minopoli Fiorella, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Nygren Gudrun, Oliveira Guiomar, Pagnamenta Alistair T, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Pickles Andrew, Pinto Dalila, Piven Joseph, Posey David J, Poustka Annemarie, Poustka Fritz, Ragoussis Jiannis, Roge Bernadette, Rutter Michael L, Sequeira Ana F, Soorya Latha, Sousa Inês, Sykes Nuala, Stoppioni Vera, Tancredi Raffaella, Tauber Maïté, Thompson Ann P, Thomson Susanne, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Vorstman Jacob A S, Wallace Simon, Wang Kai, Wassink Thomas H, White Kathy, Wing Kirsty, Wittemeyer Kerstin, Yaspan Brian L, Zwaigenbaum Lonnie, Betancur Catalina, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Geschwind Daniel H, Haines Jonathan L, Hallmayer Joachim, Monaco Anthony P, Nurnberger John I, Pericak-Vance Margaret A, Schellenberg Gerard D, Scherer Stephen W, Sutcliffe James S, Szatmari Peter, Vieland Veronica J, Wijsman Ellen M, Green Andrew, Gill Michael, Gallagher Louise, Vicente Astrid and Ennis Sean. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. : Human genetics. 20120514.