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Publications by Carol Nelson‐Williams

SLC12A Ion Transporter Mutations in Sporadic and Familial Human Congenital Hydrocephalus

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

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Sporadic and Familial Cases of Aquagenic Keratoderma

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De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus

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Congenital Familial Nodal Rhythm

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2.Congenital Hydrocephalus : Standard Treatment and Its Result

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