Pages that link to "Q29544005"
Jump to navigation
Jump to search
The following pages link to Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size (Q29544005):
Displaying 50 items.
- Genome-wide copy number analysis uncovers a new HSCR gene: NRG3 (Q21144917) (← links)
- The genetics of attention deficit/hyperactivity disorder in adults, a review (Q22251103) (← links)
- Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome. (Q24604419) (← links)
- Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder (Q24604488) (← links)
- Doc2 supports spontaneous synaptic transmission by a Ca(2+)-independent mechanism (Q26269899) (← links)
- Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology (Q26770773) (← links)
- Characterizing autism spectrum disorders by key biochemical pathways (Q26781645) (← links)
- Synaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia (Q26829347) (← links)
- Copy number variants in obesity-related syndromes: review and perspectives on novel molecular approaches (Q27005637) (← links)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics (Q27022289) (← links)
- Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes (Q27309937) (← links)
- Phenotypic Consequences of Copy Number Variation: Insights from Smith-Magenis and Potocki-Lupski Syndrome Mouse Models (Q27322785) (← links)
- A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men (Q27333802) (← links)
- Structural variation mutagenesis of the human genome: Impact on disease and evolution (Q27691419) (← links)
- Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms (Q28087577) (← links)
- Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications (Q28304430) (← links)
- GABAB Receptor Agonist R-Baclofen Reverses Social Deficits and Reduces Repetitive Behavior in Two Mouse Models of Autism (Q28391720) (← links)
- Mosaic structural variation in children with developmental disorders (Q28392317) (← links)
- Comprehensive Analysis of the 16p11.2 Deletion and Null Cntnap2 Mouse Models of Autism Spectrum Disorder (Q28547298) (← links)
- Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder (Q28943293) (← links)
- Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting (Q29616013) (← links)
- A Nondegenerate Code of Deleterious Variants in Mendelian Loci Contributes to Complex Disease Risk (Q30002401) (← links)
- 16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions. (Q30362781) (← links)
- 16p11.2 Deletion mice display cognitive deficits in touchscreen learning and novelty recognition tasks (Q30390740) (← links)
- Using whole-exome sequencing to identify inherited causes of autism (Q30418126) (← links)
- Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome (Q30423739) (← links)
- A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2. (Q30699408) (← links)
- The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population (Q30847370) (← links)
- Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence (Q33581309) (← links)
- Mosaicism for structural non-centromeric autosomal rearrangements in disease-defined carriers: sex differences in the rearrangements profile and maternal age distributions (Q33709196) (← links)
- Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11. (Q33741872) (← links)
- Structural variation and missense mutation in SBDS associated with Shwachman-Diamond syndrome (Q33756158) (← links)
- Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice. (Q33772616) (← links)
- Identification of a novel methylated gene in nasopharyngeal carcinoma: TTC40 (Q33912110) (← links)
- Genomics, intellectual disability, and autism (Q33937230) (← links)
- Genetic architectures of psychiatric disorders: the emerging picture and its implications (Q33949729) (← links)
- The genetics of Autism Spectrum Disorders--a guide for clinicians (Q34034825) (← links)
- CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree. (Q34055765) (← links)
- Opposing brain differences in 16p11.2 deletion and duplication carriers (Q34067282) (← links)
- Are copy number variants associated with adolescent idiopathic scoliosis? (Q34161281) (← links)
- Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic Behavior (Q34188749) (← links)
- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus (Q34212342) (← links)
- The imprinted brain: how genes set the balance between autism and psychosis (Q34236353) (← links)
- MLPA for confirmation of array CGH results and determination of inheritance (Q34243058) (← links)
- Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk? (Q34249436) (← links)
- The effect of homozygous deletion of the BBOX1 and Fibin genes on carnitine level and acyl carnitine profile (Q34285719) (← links)
- Animal models of psychiatric disorders that reflect human copy number variation. (Q34294530) (← links)
- Genetic insights into the functional elements of language (Q34349576) (← links)
- The genomics of schizophrenia: update and implications. (Q34381708) (← links)
- Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problems. (Q34381783) (← links)