developmental delay

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malformations of cortical development: genetic mechanisms and diagnostic approach
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3
Partial Trisomy of Chromosome 13 with a Novel Translocation (8 ; 13) and Unique Clinical Presentation in a Palestinian Infant
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The effectiveness of an embedded programme to increase the linguistic responsiveness of caregivers in an orphanage in South Africa.
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7
Xq22 deletions and correlation with distinct neurological disease traits in females: further evidence for a contiguous gene syndrome.
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Validation of the Quantitative Checklist for Autism in Toddlers in an Italian Clinical Sample of Young Children With Autism and Other Developmental Disorders.
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10
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy.
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11
Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.
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12
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13
Impact of Intrauterine Growth Restriction on Cognitive and Motor Development at 2 Years of Age.
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14
A 46,XY Female with a 9p24.3p24.1 Deletion and a 8q24.11q24.3 Duplication: A Case Report and Review of the Literature.
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15
Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin.
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16
Developmental outcomes following prenatal exposure to methamphetamine: A Western Australian perspective.
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17
Mortality and neurodevelopmental outcomes of acute bacterial meningitis in children aged <5 years in Pakistan.
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18
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Development of sleep-wake rhythms during the first year of age.
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20
Clinical Usefulness of the Korean Developmental Screening Test (K-DST) for Developmental Delays.
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epilepsy cerebral cortex neurogenesispediatrics