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Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder
Clinical Genetics
◽
10.1111/cge.13851
◽
2020
◽
Vol 98
(6)
◽
pp. 571-576
Author(s):
Nina B. Gold
◽
Dong Li
◽
Anna Chassevent
◽
Frank J. Kaiser
◽
Ilaria Parenti
◽
...
Keyword(s):
Autism Spectrum Disorder
◽
Developmental Delay
◽
De Novo
◽
Autism Spectrum
◽
Spectrum Disorder
Download Full-text
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References
De novo exon 1 deletion ofAUTS2gene in a patient with autism spectrum disorder and developmental delay: A case report and a brief literature review
American Journal of Medical Genetics Part A
◽
10.1002/ajmg.a.37050
◽
2015
◽
Vol 167
(6)
◽
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◽
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Author(s):
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◽
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◽
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◽
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◽
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◽
...
Keyword(s):
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◽
Case Report
◽
Literature Review
◽
Developmental Delay
◽
De Novo
◽
Autism Spectrum
◽
Spectrum Disorder
◽
Exon 1
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A de novo TOP2B variant associated with global developmental delay and autism spectrum disorder
Molecular Genetics & Genomic Medicine
◽
10.1002/mgg3.1145
◽
2020
◽
Vol 8
(3)
◽
Author(s):
Takuya Hiraide
◽
Seiji Watanabe
◽
Tomoko Matsubayashi
◽
Kumiko Yanagi
◽
Mitsuko Nakashima
◽
...
Keyword(s):
Autism Spectrum Disorder
◽
Developmental Delay
◽
De Novo
◽
Autism Spectrum
◽
Spectrum Disorder
◽
Global Developmental Delay
Download Full-text
Review for "Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder"
10.1111/cge.13851/v2/review1
◽
2020
◽
Keyword(s):
Autism Spectrum Disorder
◽
Developmental Delay
◽
De Novo
◽
Autism Spectrum
◽
Spectrum Disorder
Download Full-text
Review for "Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder"
10.1111/cge.13851/v1/review2
◽
2020
◽
Keyword(s):
Autism Spectrum Disorder
◽
Developmental Delay
◽
De Novo
◽
Autism Spectrum
◽
Spectrum Disorder
Download Full-text
Decision letter for "Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder"
10.1111/cge.13851/v2/decision1
◽
2020
◽
Keyword(s):
Autism Spectrum Disorder
◽
Developmental Delay
◽
De Novo
◽
Autism Spectrum
◽
Spectrum Disorder
Download Full-text
Haploinsufficiency of CMIP in a Girl With Autism Spectrum Disorder and Developmental Delay due to a De Novo Deletion on Chromosome 16q23.2
Autism Research
◽
10.1002/aur.1240
◽
2012
◽
Vol 5
(4)
◽
pp. 277-281
◽
Cited By ~ 16
Author(s):
Nathalie Van der Aa
◽
Geert Vandeweyer
◽
Edwin Reyniers
◽
Sandra Kenis
◽
Lina Dom
◽
...
Keyword(s):
Autism Spectrum Disorder
◽
Developmental Delay
◽
De Novo
◽
Autism Spectrum
◽
Spectrum Disorder
Download Full-text
Author response for "Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder"
10.1111/cge.13851/v2/response1
◽
2020
◽
Author(s):
Nina B. Gold
◽
Dong Li
◽
Anna Chassevent
◽
Frank J. Kaiser
◽
Ilaria Parenti
◽
...
Keyword(s):
Autism Spectrum Disorder
◽
Developmental Delay
◽
De Novo
◽
Autism Spectrum
◽
Spectrum Disorder
◽
Author Response
Download Full-text
Review for "Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder"
10.1111/cge.13851/v1/review1
◽
2020
◽
Keyword(s):
Autism Spectrum Disorder
◽
Developmental Delay
◽
De Novo
◽
Autism Spectrum
◽
Spectrum Disorder
Download Full-text
Decision letter for "Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder"
10.1111/cge.13851/v1/decision1
◽
2020
◽
Keyword(s):
Autism Spectrum Disorder
◽
Developmental Delay
◽
De Novo
◽
Autism Spectrum
◽
Spectrum Disorder
Download Full-text
Developmental delay with autism spectrum disorder and gait instability
10.32388/6mudd1
◽
2020
◽
Author(s):
Keyword(s):
Autism Spectrum Disorder
◽
Developmental Delay
◽
Autism Spectrum
◽
Spectrum Disorder
Download Full-text
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