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2018
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Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.
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S-EPMC5933354
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biostudies-literature
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Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.
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S-EPMC5360844
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biostudies-literature
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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
Not available
S-EPMC3637175
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biostudies-literature
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