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Incidence of thrombocytopenia in infants born to mothers with idiopathic thrombocytopenic purpura

โœ Scribed by Takeshi Asano; Rintaro Sawa; Tsutomu Arakf; Masao Yamamoto


Book ID
108970671
Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
278 KB
Volume
40
Category
Article
ISSN
1328-8067

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The phenotypic spectrum caused by the microdeletion of chromosome 22q11 region is known to be variable. Nearly all patients with DiGeorge sequence (DGS) and approximately 60% of patients with velocardiofacial syndrome exhibit the deletion. Recent papers have reported various congenital defects in pa