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Integrated Gene Analyses Of De Novo Variants From 46612 Trios With Autism And Developmental
Regulatory De Novo Mutations Underlying Intellectual Disability Life Science Alliance
Regulatory De Novo Mutations Underlying Intellectual Disability Life Science Alliance
Regulatory De Novo Mutations Underlying Intellectual Disability Life Science Alliance
Regulatory De Novo Mutations Underlying Intellectual Disability Life Science Alliance
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Frontiers De Novo Mutations Dnms In Autism Spectrum Disorder Asd Pathway And Network Analysis
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Pdf Strategies To Advance Drug Discovery In Rare Monogenic Intellectual Disability Syndromes
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Pdf De Novo Variants In Chinese Asd Trios Reveal Distinct Genetic Basis Underlying Autism With
Integrated Gene Analyses Of De Novo Variants From 46612 Trios With Autism And Developmental
Integrated Gene Analyses Of De Novo Variants From 46612 Trios With Autism And Developmental
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Pdf Regulatory De Novo Mutations Underlying Intellectual Disability
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Pdf Novel Candidate Genes And Variants Underlying Autosomal Recessive Neurodevelopmental
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Truncating Variants In Naa15 Are Associated With Variable Levels Of Intellectual Disability
Sex Based Analysis Of De Novo Variants In Neurodevelopmental Disorders The American Journal Of
Sex Based Analysis Of De Novo Variants In Neurodevelopmental Disorders The American Journal Of
Figure 1 From A De Novo Mutation In The X Linked Pak3 Gene Is The Underlying Cause Of
Figure 1 From A De Novo Mutation In The X Linked Pak3 Gene Is The Underlying Cause Of
Regulatory De Novo Mutations Underlying Intellectual Disability Life Science Alliance
Regulatory De Novo Mutations Underlying Intellectual Disability Life Science Alliance
Pdf Usp27x Variants Underlying X Linked Intellectual Disability Disrupt Protein Function Via
Pdf Usp27x Variants Underlying X Linked Intellectual Disability Disrupt Protein Function Via
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De Novo Variants Underlying Monogenic Syndromes With Intellectual Disability In A
Regulatory De Novo Mutations Underlying Intellectual Disability Life Science Alliance
Regulatory De Novo Mutations Underlying Intellectual Disability Life Science Alliance
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De Novo Variants In Ebf3 Are Associated With Hypotonia Developmental Delay Intellectual
De Novo Truncating Variants In Son Cause Intellectual Disability Congenital Malformations And
De Novo Truncating Variants In Son Cause Intellectual Disability Congenital Malformations And
Genematcher Aids In The Identification Of A New Malformation Syndrome With Intellectual
Genematcher Aids In The Identification Of A New Malformation Syndrome With Intellectual
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Pdf De Novo Variants Underlying Monogenic Syndromes With Intellectual Disability In A
Regulatory De Novo Mutations Underlying Intellectual Disability Life Science Alliance
Regulatory De Novo Mutations Underlying Intellectual Disability Life Science Alliance
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De Novo And Bi Allelic Variants In Ap1g1 Cause Neurodevelopmental Disorder With Developmental
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Pdf De Novo And Inherited Tcf20 Pathogenic Variants Are Associated With Intellectual
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Pdf Novel Candidate Genes And Variants Underlying Autosomal Recessive Neurodevelopmental
Monogenic Syndromes With Associated Cdh Caused By De Novo Events Download Scientific Diagram
Monogenic Syndromes With Associated Cdh Caused By De Novo Events Download Scientific Diagram
Integrated Gene Analyses Of De Novo Variants From 46612 Trios With Autism And Developmental
Integrated Gene Analyses Of De Novo Variants From 46612 Trios With Autism And Developmental
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Pdf Correction To De Novo And Inherited Tcf20 Pathogenic Variants Are Associated With
Pdf De Novo Variants In Neurodevelopmental Disorders Experiences From A Tertiary Care Center
Pdf De Novo Variants In Neurodevelopmental Disorders Experiences From A Tertiary Care Center
De Novo And Inherited Tcf20 Pathogenic Variants Are Associated With Intellectual Disability
De Novo And Inherited Tcf20 Pathogenic Variants Are Associated With Intellectual Disability
Frontiers De Novo Mutations Genetic Mosaicism And Human Disease
Frontiers De Novo Mutations Genetic Mosaicism And Human Disease
De Novo Variants In Camta1 Cause A Syndrome Variably Associated With Spasticity Ataxia And
De Novo Variants In Camta1 Cause A Syndrome Variably Associated With Spasticity Ataxia And
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Pdf Novel Variants Underlying Autosomal Recessive Neurodevelopmental Disorders With
Pdf Heterozygous Ankrd17 Loss Of Function Variants Cause A Syndrome With Intellectual
Pdf Heterozygous Ankrd17 Loss Of Function Variants Cause A Syndrome With Intellectual
