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The Journal of Heredity|August 18, 2011
Lix1 knockout mouse does not exhibit spinal muscular atrophy phenotypeErin N Wakeling, John C Fyfe
The Journal of Molecular Diagnostics : JMD|October 14, 2014
Extra alleles in FMR1 triple-primed PCR: artifact, aneuploidy, or somatic mosaicism?Erin N Wakeling, Fatimah A Nahhas, Gerald L Feldman
The Journal of Comparative Neurology|November 29, 2011
Failure of lower motor neuron radial outgrowth precedes retrograde degeneration in a feline model of spinal muscular atrophyErin N Wakeling, Béatrice Joussemet, Patrick Costiou, et al.
Pediatric Hematology and Oncology|September 29, 2020
Distinctive phenotypes in two children with novel germline <i>RUNX1</i> mutations - one with myeloid malignancy and increased fetal hemoglobinShruti Bagla, Katherine A Regling, Erin N Wakeling, et al.
European Journal of Human Genetics : EJHG|March 20, 2025
Heterozygous CELF4 variants in the N-term region crucial for the RNA-binding activity lead to neurodevelopmental disorder and obesityAnge-Line Bruel, Anneke T Vulto-vanSilfhout, Frédéric Bilan, et al.
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