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Paper Details

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?
Am J Med Genet A
16
2017
FOX, FOXP1, FOXP1 haploinsufficiency, Foxp1, NEHI, NM_, NM_032682.5:, autism spectrum disorder, cardiomyocytes, congenital anomalies of the kidney and, edema, facial dysmorphisms, flushing, forkhead box, humans, intellectual disability, language and speech defects, lung disease, lymphocytes, mice, neuroendocrine cell hyperplasia of infancy, patients, skeletal disorder, spinal motor neurons, undertubulation of the long bones
Author NameAffiliation
Christ??le du SouichUniversity of British Columbia
Christ??le du SouichBC Children's Hospital Research Institute
Cornelius F BoerkoelUniversity of South Dakota and Sanford Health
Cornelius F BoerkoelUniversity of British Columbia
Cornelius F BoerkoelBC Children's Hospital Research Institute
Cornelius F BoerkoelUniversity of South Dakota and Sanford Health
Cornelius F BoerkoelUniversity of British Columbia
Cornelius F BoerkoelBC Children's Hospital Research Institute
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