APA
Reijnders M. R. F., Miller K. A., Alvi M., Goos J. A. C., Lees M. M., de Burca A., Henderson A., Kraus A., Mikat B., de Vries B. B. A., Isidor B., Kerr B., Marcelis C., Schluth-Bolard C., Deshpande C., Ruivenkamp C. A. L., Wieczorek D., Baralle D., Blair E. M., Engels H., Lüdecke H., Eason J., Santen G. W. E., Clayton-Smith J., Chandler K., Tatton-Brown K., Payne K., Helbig K., Radtke K., Nugent K. M., Cremer K., Strom T. M., Bird L. M., Sinnema M., Bitner-Glindzicz M., van Dooren M. F., Alders M., Koopmans M., Brick L., Kozenko M., Harline M. L., Klaassens M., Steinraths M., Cooper N. S., Edery P., Yap P., Terhal P. A., van der Spek P. J., Lakeman P., Taylor R. L., Littlejohn R. O., Pfundt R., Mercimek-Andrews S., Stegmann A. P. A., Kant S. G., McLean S., Joss S., Swagemakers S. M. A., Douzgou S., Wall S. A., Küry S., Calpena E., Koelling N., McGowan S. J., Twigg S. R. F., Mathijssen I. M. J., Nellaker C., Brunner H. G. & Wilkie A. O. M. (20181211). De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder. : American journal of human genetics.
Chicago
Reijnders Margot R F, Miller Kerry A, Alvi Mohsan, Goos Jacqueline A C, Lees Melissa M, de Burca Anna, Henderson Alex, Kraus Alison, Mikat Barbara, de Vries Bert B A, Isidor Bertrand, Kerr Bronwyn, Marcelis Carlo, Schluth-Bolard Caroline, Deshpande Charu, Ruivenkamp Claudia A L, Wieczorek Dagmar, Baralle Diana, Blair Edward M, Engels Hartmut, Lüdecke Hermann-Josef, Eason Jacqueline, Santen Gijs W E, Clayton-Smith Jill, Chandler Kate, Tatton-Brown Katrina, Payne Katelyn, Helbig Katherine, Radtke Kelly, Nugent Kimberly M, Cremer Kirsten, Strom Tim M, Bird Lynne M, Sinnema Margje, Bitner-Glindzicz Maria, van Dooren Marieke F, Alders Marielle, Koopmans Marije, Brick Lauren, Kozenko Mariya, Harline Megan L, Klaassens Merel, Steinraths Michelle, Cooper Nicola S, Edery Patrick, Yap Patrick, Terhal Paulien A, van der Spek Peter J, Lakeman Phillis, Taylor Rachel L, Littlejohn Rebecca O, Pfundt Rolph, Mercimek-Andrews Saadet, Stegmann Alexander P A, Kant Sarina G, McLean Scott, Joss Shelagh, Swagemakers Sigrid M A, Douzgou Sofia, Wall Steven A, Küry Sébastien, Calpena Eduardo, Koelling Nils, McGowan Simon J, Twigg Stephen R F, Mathijssen Irene M J, Nellaker Christoffer, Brunner Han G and Wilkie Andrew O M. 20181211. De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder. : American journal of human genetics.
Harvard
Reijnders M. R. F., Miller K. A., Alvi M., Goos J. A. C., Lees M. M., de Burca A., Henderson A., Kraus A., Mikat B., de Vries B. B. A., Isidor B., Kerr B., Marcelis C., Schluth-Bolard C., Deshpande C., Ruivenkamp C. A. L., Wieczorek D., Baralle D., Blair E. M., Engels H., Lüdecke H., Eason J., Santen G. W. E., Clayton-Smith J., Chandler K., Tatton-Brown K., Payne K., Helbig K., Radtke K., Nugent K. M., Cremer K., Strom T. M., Bird L. M., Sinnema M., Bitner-Glindzicz M., van Dooren M. F., Alders M., Koopmans M., Brick L., Kozenko M., Harline M. L., Klaassens M., Steinraths M., Cooper N. S., Edery P., Yap P., Terhal P. A., van der Spek P. J., Lakeman P., Taylor R. L., Littlejohn R. O., Pfundt R., Mercimek-Andrews S., Stegmann A. P. A., Kant S. G., McLean S., Joss S., Swagemakers S. M. A., Douzgou S., Wall S. A., Küry S., Calpena E., Koelling N., McGowan S. J., Twigg S. R. F., Mathijssen I. M. J., Nellaker C., Brunner H. G. and Wilkie A. O. M. (20181211). De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder. : American journal of human genetics.
MLA
Reijnders Margot R F, Miller Kerry A, Alvi Mohsan, Goos Jacqueline A C, Lees Melissa M, de Burca Anna, Henderson Alex, Kraus Alison, Mikat Barbara, de Vries Bert B A, Isidor Bertrand, Kerr Bronwyn, Marcelis Carlo, Schluth-Bolard Caroline, Deshpande Charu, Ruivenkamp Claudia A L, Wieczorek Dagmar, Baralle Diana, Blair Edward M, Engels Hartmut, Lüdecke Hermann-Josef, Eason Jacqueline, Santen Gijs W E, Clayton-Smith Jill, Chandler Kate, Tatton-Brown Katrina, Payne Katelyn, Helbig Katherine, Radtke Kelly, Nugent Kimberly M, Cremer Kirsten, Strom Tim M, Bird Lynne M, Sinnema Margje, Bitner-Glindzicz Maria, van Dooren Marieke F, Alders Marielle, Koopmans Marije, Brick Lauren, Kozenko Mariya, Harline Megan L, Klaassens Merel, Steinraths Michelle, Cooper Nicola S, Edery Patrick, Yap Patrick, Terhal Paulien A, van der Spek Peter J, Lakeman Phillis, Taylor Rachel L, Littlejohn Rebecca O, Pfundt Rolph, Mercimek-Andrews Saadet, Stegmann Alexander P A, Kant Sarina G, McLean Scott, Joss Shelagh, Swagemakers Sigrid M A, Douzgou Sofia, Wall Steven A, Küry Sébastien, Calpena Eduardo, Koelling Nils, McGowan Simon J, Twigg Stephen R F, Mathijssen Irene M J, Nellaker Christoffer, Brunner Han G and Wilkie Andrew O M. De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder. : American journal of human genetics. 20181211.