APA

Reijnders M. R. F., Janowski R., Alvi M., Self J. E., van Essen T. J., Vreeburg M., Rouhl R. P. W., Stevens S. J. C., Stegmann A. P. A., Schieving J., Pfundt R., van Dijk K., Smeets E., Stumpel C. T. R. M., Bok L. A., Cobben J. M., Engelen M., Mansour S., Whiteford M., Chandler K. E., Douzgou S., Cooper N. S., Tan E., Foo R., Lai A. H. M., Rankin J., Green A., Lönnqvist T., Isohanni P., Williams S., Ruhoy I., Carvalho K. S., Dowling J. J., Lev D. L., Sterbova K., Lassuthova P., Neupauerová J., Waugh J. L., Keros S., Clayton-Smith J., Smithson S. F., Brunner H. G., van Hoeckel C., Anderson M., Clowes V. E., Siu V. M., Ddd Study T., Selber P., Leventer R. J., Nellaker C., Niessing D., Hunt D. & Baralle D. (20190910). PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature. : Journal of medical genetics.

Chicago

Reijnders Margot R F, Janowski Robert, Alvi Mohsan, Self Jay E, van Essen Ton J, Vreeburg Maaike, Rouhl Rob P W, Stevens Servi J C, Stegmann Alexander P A, Schieving Jolanda, Pfundt Rolph, van Dijk Katinke, Smeets Eric, Stumpel Connie T R M, Bok Levinus A, Cobben Jan Maarten, Engelen Marc, Mansour Sahar, Whiteford Margo, Chandler Kate E, Douzgou Sofia, Cooper Nicola S, Tan Ene-Choo, Foo Roger, Lai Angeline H M, Rankin Julia, Green Andrew, Lönnqvist Tuula, Isohanni Pirjo, Williams Shelley, Ruhoy Ilene, Carvalho Karen S, Dowling James J, Lev Dorit L, Sterbova Katalin, Lassuthova Petra, Neupauerová Jana, Waugh Jeff L, Keros Sotirios, Clayton-Smith Jill, Smithson Sarah F, Brunner Han G, van Hoeckel Ceciel, Anderson Mel, Clowes Virginia E, Siu Victoria Mok, Ddd Study The, Selber Paulo, Leventer Richard J, Nellaker Christoffer, Niessing Dierk, Hunt David and Baralle Diana. 20190910. PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature. : Journal of medical genetics.

Harvard

Reijnders M. R. F., Janowski R., Alvi M., Self J. E., van Essen T. J., Vreeburg M., Rouhl R. P. W., Stevens S. J. C., Stegmann A. P. A., Schieving J., Pfundt R., van Dijk K., Smeets E., Stumpel C. T. R. M., Bok L. A., Cobben J. M., Engelen M., Mansour S., Whiteford M., Chandler K. E., Douzgou S., Cooper N. S., Tan E., Foo R., Lai A. H. M., Rankin J., Green A., Lönnqvist T., Isohanni P., Williams S., Ruhoy I., Carvalho K. S., Dowling J. J., Lev D. L., Sterbova K., Lassuthova P., Neupauerová J., Waugh J. L., Keros S., Clayton-Smith J., Smithson S. F., Brunner H. G., van Hoeckel C., Anderson M., Clowes V. E., Siu V. M., Ddd Study T., Selber P., Leventer R. J., Nellaker C., Niessing D., Hunt D. and Baralle D. (20190910). PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature. : Journal of medical genetics.

MLA

Reijnders Margot R F, Janowski Robert, Alvi Mohsan, Self Jay E, van Essen Ton J, Vreeburg Maaike, Rouhl Rob P W, Stevens Servi J C, Stegmann Alexander P A, Schieving Jolanda, Pfundt Rolph, van Dijk Katinke, Smeets Eric, Stumpel Connie T R M, Bok Levinus A, Cobben Jan Maarten, Engelen Marc, Mansour Sahar, Whiteford Margo, Chandler Kate E, Douzgou Sofia, Cooper Nicola S, Tan Ene-Choo, Foo Roger, Lai Angeline H M, Rankin Julia, Green Andrew, Lönnqvist Tuula, Isohanni Pirjo, Williams Shelley, Ruhoy Ilene, Carvalho Karen S, Dowling James J, Lev Dorit L, Sterbova Katalin, Lassuthova Petra, Neupauerová Jana, Waugh Jeff L, Keros Sotirios, Clayton-Smith Jill, Smithson Sarah F, Brunner Han G, van Hoeckel Ceciel, Anderson Mel, Clowes Virginia E, Siu Victoria Mok, Ddd Study The, Selber Paulo, Leventer Richard J, Nellaker Christoffer, Niessing Dierk, Hunt David and Baralle Diana. PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature. : Journal of medical genetics. 20190910.