A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing.

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FAM20A Gene Mutation: Amelogenesis or Ectopic Mineralization?Amelogenesis Imperfecta; Genes, Proteins, and Pathways.

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A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing.

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A distinctive oral phenotype p ...... entified by Sanger sequencing.

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A distinctive oral phenotype p ...... entified by Sanger sequencing.

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A distinctive oral phenotype p ...... entified by Sanger sequencing.

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A distinctive oral phenotype p ...... entified by Sanger sequencing.

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A distinctive oral phenotype p ...... entified by Sanger sequencing.

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A distinctive oral phenotype p ...... entified by Sanger sequencing.

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A distinctive oral phenotype p ...... entified by Sanger sequencing.

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Claire E L Smith

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Gina Murrillo

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Laura Crinnion

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Marianella Howell

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Sally Feather

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Sandra Silva

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P2860

FAM20A mutations can cause enamel-renal syndrome (ERS).

Novel FAM20A mutations in hypoplastic amelogenesis imperfecta

Autosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A gene

Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease

Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations

Secreted kinase phosphorylates extracellular proteins that regulate biomineralization

A secretory kinase complex regulates extracellular protein phosphorylation

Fast and accurate short read alignment with Burrows-Wheeler transform

Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development

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scholarly article

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10.1002/MGG3.164

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A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing.

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P2860

P2860

A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing.

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P1476

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P2860

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