DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Bengoa-Alonso A, Artigas-López M, Moreno-Igoa M, Cattalli C, Hernández-Charro B, Ramos-Arroyo MA.
Delineation of a recognizable phenotype for the recurrent LCR22-C to D/E atypical 22q11.2 deletion.
Am J Med Genet A 2016;
170 (06) 1485-1494
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