Jessica Pfliger

Affiliations: 
2022- Baylor College of Medicine, Houston, TX 
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"Jessica Pfliger"
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Paul MS, Michener SL, Pan H, et al. (2024) A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3. American Journal of Human Genetics
Paul MS, Michener SL, Pan H, et al. (2024) A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3. American Journal of Human Genetics
Paul MS, Michener SL, Pan H, et al. (2024) A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3. American Journal of Human Genetics. 111: 96-118
Paul MS, Michener SL, Pan H, et al. (2023) Rare variants in cause delayed development, intellectual disability, autism, and epilepsy. Medrxiv : the Preprint Server For Health Sciences
Deisseroth CA, Lerma VC, Magyar CL, et al. (2022) An integrated phenotypic and genotypic approach reveals a high-risk subtype association for EBF3 missense variants affecting the zinc finger domain. Annals of Neurology
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