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1 editary disorders, such as spherocytosis and elliptocytosis.
2 emolytic disorders such as spherocytosis and elliptocytosis.
3 m patients with hereditary spherocytosis and elliptocytosis.
4 shape including hereditary spherocytosis and elliptocytosis.
5 ned from subjects with homozygous hereditary elliptocytosis.
6 iseases such as hereditary spherocytosis and elliptocytosis.
7 osome 4, closely linked to D4Mit16 and Elp1 (elliptocytosis-1), by using genomic DNAs from a (C57BL/6
8 died this developmental switch in hereditary elliptocytosis 4.1Alg, in which a DNA rearrangement invo
10 y about the resulting conditions (hereditary elliptocytosis and pyropoikilocytosis), the detailed str
11 itary blood disorders such as spherocytosis, elliptocytosis, and especially, sickle cell disease requ
12 such as hereditary spherocytosis, hereditary elliptocytosis, and hereditary pyropoikilocytosis, are c
17 hereditary spherocytosis (HS) and hereditary elliptocytosis (HE), deficiencies of membrane proteins,
18 a variety of syndromes, including hereditary elliptocytosis (HE), hereditary pyropoikilocytosis (HPP)
19 rin dimers to tetramers result in hereditary elliptocytosis (HE), whereas a deficiency of human eryth
20 logies (hereditary spherocytosis, hereditary elliptocytosis, hereditary hydrocytosis, Southeast Asian
21 h features resembling hereditary spherocytic elliptocytosis, including decreased RBC mean corpuscular
22 r formation site, modeled after a hereditary elliptocytosis mutation in human erythrocyte spectrin, h
25 etry characterization of a common hereditary elliptocytosis-related mutation of alpha-spectrin, L207P
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