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Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation.
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Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation.
Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation. Mol Genet Genomic Med. 2019 03; 7(3):e549.
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PubMed
subject areas
Adolescent
Adult
Aged
Alleles
Child
Child, Preschool
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 18
De Lange Syndrome
Digestive System Abnormalities
DNA Copy Number Variations
Female
Humans
Infant
Infant, Newborn
Intestinal Volvulus
Male
Middle Aged
Williams Syndrome
authors with profiles
PAWEL STANKIEWICZ
PRZEMYSLAW SZAFRANSKI