Search Results - Malallah, Asma Jassim

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    Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His

    Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His by Alsada, Maryam, Khan, Farheen, Malallah, Asma Jassim, Aashiq, Mohamed

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    Early severe neonatal hyperbilirubinaemia associated with congenital hypothyroidism treated with exchange transfusions

    Early severe neonatal hyperbilirubinaemia associated with congenital hypothyroidism treated with exchange transfusions by Khan, Anwar, Iqbal, Khalid, Galal, Mahmoud, Malallah, Asma Jassim, Zein, Nada

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    Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His

    Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His by Aashiq, Mohamed, Malallah, Asma Jassim, Khan, Farheen, Alsada, Maryam

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