ZMYND11-related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum. [electronic resource]
Producer: 20210721Description: 1042-1050 p. digitalISSN:- 1098-1004
- Alleles
- Cell Cycle Proteins -- genetics
- Child
- Child, Preschool
- Co-Repressor Proteins -- genetics
- DNA-Binding Proteins -- genetics
- Facies
- Female
- Genetic Association Studies -- methods
- Genetic Predisposition to Disease
- Genotype
- Haploinsufficiency
- Humans
- Intellectual Disability -- diagnosis
- Male
- Mutation
- Nonsense Mediated mRNA Decay
- Phenotype
- Syndrome
- Zinc Fingers
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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