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UnknownClassification and stratification in pilonidal sinus disease: findings from the PITSTOP cohort.
Not available
S-EPMC11683182 | biostudies-literature
UnknownClinical phenotype of the recurrent 1q21.1 copy-number variant.
Not available
S-EPMC7263044 | biostudies-literature
UnknownThe cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Not available
S-EPMC5410712 | biostudies-literature
UnknownA 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Not available
S-EPMC3494011 | biostudies-literature
UnknownEffects of eight neuropsychiatric copy number variants on human brain structure.
Not available
S-EPMC8292542 | biostudies-literature
UnknownDefining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
Not available
S-EPMC5894477 | biostudies-literature
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