APA

Harvard C., Malenfant P., Koochek M., Creighton S., Mickelson E. C. R., Holden J. J. A., Lewis M. E. S. & Rajcan-Separovic E. (20050616). A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH. : Clinical genetics.

Chicago

Harvard C, Malenfant P, Koochek M, Creighton S, Mickelson E C R, Holden J J A, Lewis M E S and Rajcan-Separovic E. 20050616. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH. : Clinical genetics.

Harvard

Harvard C., Malenfant P., Koochek M., Creighton S., Mickelson E. C. R., Holden J. J. A., Lewis M. E. S. and Rajcan-Separovic E. (20050616). A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH. : Clinical genetics.

MLA

Harvard C, Malenfant P, Koochek M, Creighton S, Mickelson E C R, Holden J J A, Lewis M E S and Rajcan-Separovic E. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH. : Clinical genetics. 20050616.