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Blood Cells, Molecules, and Diseases, Vol. 28, Iss. 2, 2002-02 ,pp. : 134-142

Academic Press

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Commentary: Congenital Transcobalamin II Deficiency Due to Errors in RNA Editing (by Qian et al.)

By Lee P.  

Blood Cells, Molecules, and Diseases, Vol. 28, Iss. 2, 2002-02 ,pp. : 143-144

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The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domain

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Use of TaqI Digestion May Lead to Incorrect Molecular Diagnosis of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

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Expression of Properdin in Complete and Incomplete Deficiency: Normal in Vitro Synthesis by Monocytes in Two Cases with Properdin Deficiency Type II Due to Distinct Mutations

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