HAGEMAN (FACTOR-XII) LOCUS ON 7Q - REPORT OF A 2ND CASE WITH DEL(7)Q35 AND NORMAL FACTOR-XII LEVEL

被引:25
作者
FRANCKE, U
机构
[1] UNIV CALIF SAN DIEGO,SCH MED,DEPT PEDIAT,SAN DIEGO,CA 92103
[2] SAN DIEGO CHILDRENS HOSP & HLTH CTR,SAN DIEGO,CA
关键词
D O I
10.1007/BF00278736
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:363 / 367
页数:5
相关论文
共 11 条
[1]   HAGEMAN TRAIT (FACTOR-XII DEFICIENCY) - PROBABLE SECOND GENOTYPE INHERITED AS AN AUTOSOMAL DOMINANT CHARACTERISTIC [J].
BENNETT, B ;
HOLT, JB ;
RATNOFF, OD ;
ROBERTS, HR .
BLOOD-THE JOURNAL OF HEMATOLOGY, 1972, 40 (03) :412-&
[2]  
BIEDERMAN B, 1978, HUM GENET, V41, P101
[3]  
BIGGS R, 1976, HUMAN BLOOD COAGULAT
[4]  
DEGROUCHY J, 1974, HUMANGENETIK, V24, P197
[5]  
HARRIS EL, 1977, CLIN GENET, V12, P233
[6]  
HOUGIE C, 1977, LANCET, V1, P93
[7]   HAGEMAN FACTOR (FACTOR 12) IN AN AFFECTED KINDRED AND IN NORMAL ADULTS [J].
KASPER, CK ;
BUECHY, DYE ;
AGGELER, PM .
BRITISH JOURNAL OF HAEMATOLOGY, 1968, 14 (05) :543-+
[8]   PARTIAL LONG ARM DELETION OF CHROMOSOME-7 - 46,XY,DEL(7)(Q32) [J].
KOUSSEFF, BG ;
HSU, LYF ;
PACIUC, S ;
HIRSCHHORN, K .
JOURNAL OF MEDICAL GENETICS, 1977, 14 (02) :144-147
[9]  
VELTKAMP JJ, 1976, LANCET, V2, P909
[10]   DETECTION OF CARRIER STATE IN HEREDITARY COAGULATION DISORDERS .2. [J].
VELTKAMP, JJ ;
DRION, EF ;
LOELIGER, EA .
THROMBOSIS ET DIATHESIS HAEMORRHAGICA, 1968, 19 (3-4) :403-+