APA
Snijders Blok L., Rousseau J., Twist J., Ehresmann S., Takaku M., Venselaar H., Rodan L. H., Nowak C. B., Douglas J., Swoboda K. J., Steeves M. A., Sahai I., Stumpel C. T. R. M., Stegmann A. P. A., Wheeler P., Willing M., Fiala E., Kochhar A., Gibson W. T., Cohen A. S. A., Agbahovbe R., Innes A. M., Au P. Y. B., Rankin J., Anderson I. J., Skinner S. A., Louie R. J., Warren H. E., Afenjar A., Keren B., Nava C., Buratti J., Isapof A., Rodriguez D., Lewandowski R., Propst J., van Essen T., Choi M., Lee S., Chae J. H., Price S., Schnur R. E., Douglas G., Wentzensen I. M., Zweier C., Reis A., Bialer M. G., Moore C., Koopmans M., Brilstra E. H., Monroe G. R., van Gassen K. L. I., van Binsbergen E., Newbury-Ecob R., Bownass L., Bader I., Mayr J. A., Wortmann S. B., Jakielski K. J., Strand E. A., Kloth K., Bierhals T., Roberts J. D., Petrovich R. M., Machida S., Kurumizaka H., Lelieveld S., Pfundt R., Jansen S., Deriziotis P., Faivre L., Thevenon J., Assoum M., Shriberg L., Kleefstra T., Brunner H. G., Wade P. A., Fisher S. E. & Campeau P. M. (20190701). CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. : Nature communications.
Chicago
Snijders Blok Lot, Rousseau Justine, Twist Joanna, Ehresmann Sophie, Takaku Motoki, Venselaar Hanka, Rodan Lance H, Nowak Catherine B, Douglas Jessica, Swoboda Kathryn J, Steeves Marcie A, Sahai Inderneel, Stumpel Connie T R M, Stegmann Alexander P A, Wheeler Patricia, Willing Marcia, Fiala Elise, Kochhar Aaina, Gibson William T, Cohen Ana S A, Agbahovbe Ruky, Innes A Micheil, Au P Y Billie, Rankin Julia, Anderson Ilse J, Skinner Steven A, Louie Raymond J, Warren Hannah E, Afenjar Alexandra, Keren Boris, Nava Caroline, Buratti Julien, Isapof Arnaud, Rodriguez Diana, Lewandowski Raymond, Propst Jennifer, van Essen Ton, Choi Murim, Lee Sangmoon, Chae Jong H, Price Susan, Schnur Rhonda E, Douglas Ganka, Wentzensen Ingrid M, Zweier Christiane, Reis André, Bialer Martin G, Moore Christine, Koopmans Marije, Brilstra Eva H, Monroe Glen R, van Gassen Koen L I, van Binsbergen Ellen, Newbury-Ecob Ruth, Bownass Lucy, Bader Ingrid, Mayr Johannes A, Wortmann Saskia B, Jakielski Kathy J, Strand Edythe A, Kloth Katja, Bierhals Tatjana, Roberts John D, Petrovich Robert M, Machida Shinichi, Kurumizaka Hitoshi, Lelieveld Stefan, Pfundt Rolph, Jansen Sandra, Deriziotis Pelagia, Faivre Laurence, Thevenon Julien, Assoum Mirna, Shriberg Lawrence, Kleefstra Tjitske, Brunner Han G, Wade Paul A, Fisher Simon E and Campeau Philippe M. 20190701. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. : Nature communications.
Harvard
Snijders Blok L., Rousseau J., Twist J., Ehresmann S., Takaku M., Venselaar H., Rodan L. H., Nowak C. B., Douglas J., Swoboda K. J., Steeves M. A., Sahai I., Stumpel C. T. R. M., Stegmann A. P. A., Wheeler P., Willing M., Fiala E., Kochhar A., Gibson W. T., Cohen A. S. A., Agbahovbe R., Innes A. M., Au P. Y. B., Rankin J., Anderson I. J., Skinner S. A., Louie R. J., Warren H. E., Afenjar A., Keren B., Nava C., Buratti J., Isapof A., Rodriguez D., Lewandowski R., Propst J., van Essen T., Choi M., Lee S., Chae J. H., Price S., Schnur R. E., Douglas G., Wentzensen I. M., Zweier C., Reis A., Bialer M. G., Moore C., Koopmans M., Brilstra E. H., Monroe G. R., van Gassen K. L. I., van Binsbergen E., Newbury-Ecob R., Bownass L., Bader I., Mayr J. A., Wortmann S. B., Jakielski K. J., Strand E. A., Kloth K., Bierhals T., Roberts J. D., Petrovich R. M., Machida S., Kurumizaka H., Lelieveld S., Pfundt R., Jansen S., Deriziotis P., Faivre L., Thevenon J., Assoum M., Shriberg L., Kleefstra T., Brunner H. G., Wade P. A., Fisher S. E. and Campeau P. M. (20190701). CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. : Nature communications.
MLA
Snijders Blok Lot, Rousseau Justine, Twist Joanna, Ehresmann Sophie, Takaku Motoki, Venselaar Hanka, Rodan Lance H, Nowak Catherine B, Douglas Jessica, Swoboda Kathryn J, Steeves Marcie A, Sahai Inderneel, Stumpel Connie T R M, Stegmann Alexander P A, Wheeler Patricia, Willing Marcia, Fiala Elise, Kochhar Aaina, Gibson William T, Cohen Ana S A, Agbahovbe Ruky, Innes A Micheil, Au P Y Billie, Rankin Julia, Anderson Ilse J, Skinner Steven A, Louie Raymond J, Warren Hannah E, Afenjar Alexandra, Keren Boris, Nava Caroline, Buratti Julien, Isapof Arnaud, Rodriguez Diana, Lewandowski Raymond, Propst Jennifer, van Essen Ton, Choi Murim, Lee Sangmoon, Chae Jong H, Price Susan, Schnur Rhonda E, Douglas Ganka, Wentzensen Ingrid M, Zweier Christiane, Reis André, Bialer Martin G, Moore Christine, Koopmans Marije, Brilstra Eva H, Monroe Glen R, van Gassen Koen L I, van Binsbergen Ellen, Newbury-Ecob Ruth, Bownass Lucy, Bader Ingrid, Mayr Johannes A, Wortmann Saskia B, Jakielski Kathy J, Strand Edythe A, Kloth Katja, Bierhals Tatjana, Roberts John D, Petrovich Robert M, Machida Shinichi, Kurumizaka Hitoshi, Lelieveld Stefan, Pfundt Rolph, Jansen Sandra, Deriziotis Pelagia, Faivre Laurence, Thevenon Julien, Assoum Mirna, Shriberg Lawrence, Kleefstra Tjitske, Brunner Han G, Wade Paul A, Fisher Simon E and Campeau Philippe M. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. : Nature communications. 20190701.