APA
Lehman N., Mazery A. C., Visier A., Baumann C., Lachesnais D., Capri Y., Toutain A., Odent S., Mikaty M., Goizet C., Taupiac E., Jacquemont M. L., Sanchez E., Schaefer E., Gatinois V., Faivre L., Minot D., Kayirangwa H., Sang K. L. Q., Boddaert N., Bayard S., Lacombe D., Moutton S., Touitou I., Rio M., Amiel J., Lyonnet S., Sanlaville D., Picot M. C. & Geneviève D. (20180430). Molecular, clinical and neuropsychological study in 31 patients with Kabuki syndrome and KMT2D mutations. : Clinical genetics.
Chicago
Lehman N, Mazery A C, Visier A, Baumann C, Lachesnais D, Capri Y, Toutain A, Odent S, Mikaty M, Goizet C, Taupiac E, Jacquemont M L, Sanchez E, Schaefer E, Gatinois V, Faivre L, Minot D, Kayirangwa H, Sang K-H L Q, Boddaert N, Bayard S, Lacombe D, Moutton S, Touitou I, Rio M, Amiel J, Lyonnet S, Sanlaville D, Picot M C and Geneviève D. 20180430. Molecular, clinical and neuropsychological study in 31 patients with Kabuki syndrome and KMT2D mutations. : Clinical genetics.
Harvard
Lehman N., Mazery A. C., Visier A., Baumann C., Lachesnais D., Capri Y., Toutain A., Odent S., Mikaty M., Goizet C., Taupiac E., Jacquemont M. L., Sanchez E., Schaefer E., Gatinois V., Faivre L., Minot D., Kayirangwa H., Sang K. L. Q., Boddaert N., Bayard S., Lacombe D., Moutton S., Touitou I., Rio M., Amiel J., Lyonnet S., Sanlaville D., Picot M. C. and Geneviève D. (20180430). Molecular, clinical and neuropsychological study in 31 patients with Kabuki syndrome and KMT2D mutations. : Clinical genetics.
MLA
Lehman N, Mazery A C, Visier A, Baumann C, Lachesnais D, Capri Y, Toutain A, Odent S, Mikaty M, Goizet C, Taupiac E, Jacquemont M L, Sanchez E, Schaefer E, Gatinois V, Faivre L, Minot D, Kayirangwa H, Sang K-H L Q, Boddaert N, Bayard S, Lacombe D, Moutton S, Touitou I, Rio M, Amiel J, Lyonnet S, Sanlaville D, Picot M C and Geneviève D. Molecular, clinical and neuropsychological study in 31 patients with Kabuki syndrome and KMT2D mutations. : Clinical genetics. 20180430.