Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study

JF McRae; S Clayton; TW Fitzgerald; J Kaplanis; E Prigmore; D Rajan; A Sifrim; S Aitken; N Akawi; M Alvi; K Ambridge; DM Barrett; T Bayzetinova; C Tayl

doi:10.1101/049056

Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study

JF McRae, S Clayton, TW Fitzgerald, J Kaplanis, E Prigmore, D Rajan, A Sifrim, S Aitken, N Akawi, M Alvi, K Ambridge, DM Barrett, T Bayzetinova, C Tayl

Manchester Institute of Education

Research output: Contribution to journal › Article

Original language	Undefined
Journal	bioRxiv
DOIs	https://doi.org/10.1101/049056
Publication status	Published - Apr 2016

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McRae, JF., Clayton, S., Fitzgerald, TW., Kaplanis, J., Prigmore, E., Rajan, D., Sifrim, A., Aitken, S., Akawi, N., Alvi, M., Ambridge, K., Barrett, DM., Bayzetinova, T., & Tayl, C. (2016). Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study. bioRxiv. https://doi.org/10.1101/049056

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title = "Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study",

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year = "2016",

month = apr,

doi = "10.1101/049056",

language = "Undefined",

journal = "bioRxiv",

issn = "2692-8205",

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TY - JOUR

T1 - Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study

AU - McRae, JF

AU - Clayton, S

AU - Fitzgerald, TW

AU - Kaplanis, J

AU - Prigmore, E

AU - Rajan, D

AU - Sifrim, A

AU - Aitken, S

AU - Akawi, N

AU - Alvi, M

AU - Ambridge, K

AU - Barrett, DM

AU - Bayzetinova, T

AU - Tayl, C

PY - 2016/4

Y1 - 2016/4

UR - http://europepmc.org/abstract/PPR/PPR34630

U2 - 10.1101/049056

DO - 10.1101/049056

M3 - Article

SN - 2692-8205

JO - bioRxiv

JF - bioRxiv

ER -

Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study

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