Journal article

SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia

Zornitza Stark, Joanna Behrsin, Trent Burgess, Anna Ritchie, Alison Yeung, Tiong Y Tan, Natasha J Brown, Ravi Savarirayan, Neil Patel

American Journal of Medical Genetics Part A | WILEY | Published : 2015

DOI: 10.1002/ajmg.a.37177

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Keywords

Pax3
Karyotype
Humans
Mutations
Hernias, Diaphragmatic, Congenital
Chromosomes, Human, Pair 22
Life Sciences & Biomedicine
9q22.3 Duplication
Chromosome Deletion
Crkl
Survival Analysis
Chromosomes, Human, Pair 9
Genetics & Heredity
Microarray Analysis
Retrospective Studies
Science & Technology
Spina-Bifida
Microdeletion
Syndrome Phenotype
Short Stature
Trisomy
Copy-Number Variants
Male
Chromosomes, Human, Pair 2
Congenital Diaphragmatic Hernia
Female
Infant
Disorders
22q11.2 Deletions
Chromosome Duplication
Inheritance Patterns
Microarray
Chromosomes, Human, Pair 15
Gene
Tbx1
Defects