INHERITANCE OF STUART DISEASE - INVESTIGATION OF A FAMILY WITH FACTOR X DEFICIENCY

被引：18

作者：

LECHLER, E

WEBSTER, WP

ROBERTS, HR

PENCIK, GD

机构：

来源：

关键词：

D O I：

10.1097/00000441-196503000-00006

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：291 / &

共 24 条

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[2] THE THROMBOPLASTIN GENERATION TEST
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[3] IMPROVEMENT OF FACTOR-X DEFICIENCY DURING PREGNANCY
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[6] CLETON FJ, 1961, THROMBOS DIATHES HAE, V5, P87
[7] DORANTES S, 1960, Bol Med Hosp Infant Mex, V17, P139
[8] GONYEA LM, 1958, J LAB CLIN MED, V51, P398
[9] STUART CLOTTING DEFECT .2. GENETIC ASPECTS OF A NEW HEMORRHAGIC STATE
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[J]. JOURNAL OF CLINICAL INVESTIGATION, 1957, 36 (03) : 497 - 503
[10] GRAHAM JB, 1960, THROMB DIATH HEAM S1, V4, P108