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  2. Details for: Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
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Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort. [electronic resource]

By:
  • Callaghan, Daniel Benjamin
Contributor(s):
  • Rogic, Sanja
  • Tan, Powell Patrick Cheng
  • Calli, Kristina
  • Qiao, Ying
  • Baldwin, Robert
  • Jacobson, Matthew
  • Belmadani, Manuel
  • Holmes, Nathan
  • Yu, Chang
  • Li, Yanchen
  • Li, Yingrui
  • Kurtzke, Franz-Edward
  • Kuzeljevic, Boris
  • Yu, An Yi
  • Hudson, Melissa
  • Mcaughton, Amy J M
  • Xu, Yuchen
  • Dionne-Laporte, Alexandre
  • Girard, Simon
  • Liang, Ping
  • Separovic, Evica Rajcan
  • Liu, Xudong
  • Rouleau, Guy
  • Pavlidis, Paul
  • Lewis, M E Suzanne
Producer: 20200817Description: 199-206 p. digitalISSN:
  • 1399-0004
Subject(s):
  • Alleles
  • Amino Acid Substitution
  • Autism Spectrum Disorder -- diagnosis
  • British Columbia
  • Cohort Studies
  • DNA Copy Number Variations
  • Female
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Genetic Variation
  • Genotype
  • Humans
  • Male
  • Mutation
  • Phenotype
  • Polymorphism, Single Nucleotide
  • Whole Genome Sequencing
Online resources:
  • Available from publisher's website
In: Clinical genetics vol. 96
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.

APA

Callaghan D. B., Rogic S., Tan P. P. C., Calli K., Qiao Y., Baldwin R., Jacobson M., Belmadani M., Holmes N., Yu C., Li Y., Li Y., Kurtzke F., Kuzeljevic B., Yu A. Y., Hudson M., Mcaughton A. J. M., Xu Y., Dionne-Laporte A., Girard S., Liang P., Separovic E. R., Liu X., Rouleau G., Pavlidis P. & Lewis M. E. S. (20200817). Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort. : Clinical genetics.

Chicago

Callaghan Daniel Benjamin, Rogic Sanja, Tan Powell Patrick Cheng, Calli Kristina, Qiao Ying, Baldwin Robert, Jacobson Matthew, Belmadani Manuel, Holmes Nathan, Yu Chang, Li Yanchen, Li Yingrui, Kurtzke Franz-Edward, Kuzeljevic Boris, Yu An Yi, Hudson Melissa, Mcaughton Amy J M, Xu Yuchen, Dionne-Laporte Alexandre, Girard Simon, Liang Ping, Separovic Evica Rajcan, Liu Xudong, Rouleau Guy, Pavlidis Paul and Lewis M E Suzanne. 20200817. Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort. : Clinical genetics.

Harvard

Callaghan D. B., Rogic S., Tan P. P. C., Calli K., Qiao Y., Baldwin R., Jacobson M., Belmadani M., Holmes N., Yu C., Li Y., Li Y., Kurtzke F., Kuzeljevic B., Yu A. Y., Hudson M., Mcaughton A. J. M., Xu Y., Dionne-Laporte A., Girard S., Liang P., Separovic E. R., Liu X., Rouleau G., Pavlidis P. and Lewis M. E. S. (20200817). Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort. : Clinical genetics.

MLA

Callaghan Daniel Benjamin, Rogic Sanja, Tan Powell Patrick Cheng, Calli Kristina, Qiao Ying, Baldwin Robert, Jacobson Matthew, Belmadani Manuel, Holmes Nathan, Yu Chang, Li Yanchen, Li Yingrui, Kurtzke Franz-Edward, Kuzeljevic Boris, Yu An Yi, Hudson Melissa, Mcaughton Amy J M, Xu Yuchen, Dionne-Laporte Alexandre, Girard Simon, Liang Ping, Separovic Evica Rajcan, Liu Xudong, Rouleau Guy, Pavlidis Paul and Lewis M E Suzanne. Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort. : Clinical genetics. 20200817.

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