A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
By L. Botto, K. May, P. Fernhoff, Adolfo Correa, K. Coleman, S. Rasmussen, Robert K Merritt, L. O’Leary, L. Wong, E. Elixson and 2 more. Pediatrics, 2003
681 citations recorded by the source corpus.
Subfields: Developmental Neuroscience, Epidemiology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/0e5e62f01ab037f26defbe597c1d151231e7b65f
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In Molecular Biology
Citations in the corpus
- Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model (2008, background): “2 locus are among the most common chromosomal abnormalitie”