Torthaí cuardaigh - Roberson, Jacquelyn

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  1. 1
    Biallelic Variants in LAMB1 Causing Hydranencephaly: A Severe Phenotype of a Rare Malformative Encephalopathy

    Biallelic Variants in LAMB1 Causing Hydranencephaly: A Severe Phenotype of a Rare Malformative Encephalopathy de réir Sen, Kuntal, Kaur, Shagun, Stockton, David W., Nyhuis, Mary, Roberson, Jacquelyn

    Foilsithe / Cruthaithe 2021
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  2. 2
    A Novel SERPINA1 Mutation Causing Serum Alpha(1)-Antitrypsin Deficiency

    A Novel SERPINA1 Mutation Causing Serum Alpha(1)-Antitrypsin Deficiency de réir Saunders, Darren N., Tindall, Elizabeth A., Shearer, Robert F., Roberson, Jacquelyn, Decker, Amy, Wilson, Jean Amos, Hayes, Vanessa M.

    Foilsithe / Cruthaithe 2012
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