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Article

Pure 21q22.3 deletion identified in a patient with mild phenotypic features.

Congenital anomalies - 1 Sept 2018

Sgardioli Ilária Cristina, Copelli Matheus de Melo, Lustosa-Mendes Elaine, Vieira Társis Paiva, Gil-da-Silva-Lopes Vera Lúcia

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Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 21
Share to Intellectual Disability
Share to Intracellular Signaling Peptides and Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Karyotyping

Share to Phenotype

Share to Protein-Arginine N-Methyltransferases

Share to Protein Serine-Threonine Kinases

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Identifiers

PMID: 29322562
DOI: 10.1111/cga.12270

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