High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan.

Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility.

Copy-number variation in the pathogenesis of autism spectrum disorder.

Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families.

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

High prevalence of pathologic copy number variants detected by chromosomal microarray in Swiss-Italian children with autism spectrum disorders.

Copy number analysis of NIPBL in a cohort of 510 patients reveals rare copy number variants and a mosaic deletion.

Copy number variation in Han Chinese individuals with autism spectrum disorder.

Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10.

Endometriosis is associated with rare copy number variants.

High-resolution assessment of copy number variation.

Rare de novo copy number variants in patients with congenital pulmonary atresia.

Cannabis abuse and age at onset in schizophrenia patients with large, rare copy number variants.

Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.

Rare copy number variation in treatment-resistant major depressive disorder.

Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general population.

Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.

Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.

Cadps2 copy number and alternative splicing variants.

The Contribution of Mosaic Variants to Autism Spectrum Disorder.

Analysis of germline gene copy number variants of patients with sporadic pancreatic adenocarcinoma reveals specific variations.

Neuroanatomical Alterations in High-Functioning Adults with Autism Spectrum Disorder.

CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data.

Mitochondrial Copy Number and D-Loop Variants in Pompe Patients.

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Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility.

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Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families.

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

High prevalence of pathologic copy number variants detected by chromosomal microarray in Swiss-Italian children with autism spectrum disorders.

Copy number analysis of NIPBL in a cohort of 510 patients reveals rare copy number variants and a mosaic deletion.

Copy number variation in Han Chinese individuals with autism spectrum disorder.

Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10.

Endometriosis is associated with rare copy number variants.

High-resolution assessment of copy number variation.

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Cannabis abuse and age at onset in schizophrenia patients with large, rare copy number variants.

Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.

Rare copy number variation in treatment-resistant major depressive disorder.

Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general population.

Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.

Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.

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Analysis of germline gene copy number variants of patients with sporadic pancreatic adenocarcinoma reveals specific variations.

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High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan.

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