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The Genetics Corner: A Mother and Child with Cleft lip and Palate Have an Atypical 1p36 Deletion that Disrupts KIF1B, a Cause of Autosomal Dominant Charcot-Marie-Tooth Disease, Type 2A1
August 31, 2021
/
16
,
Case Report
,
ENT (Ears, Nose, Throat)
,
Genetic
,
Neurology
,
Surgery/Surgical
Subhadra Ramanathan, MSc MS, Robin Dawn Clark, MD
nt-21-08-118-121
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