PARTIAL DEFICIENCY OF COAGULATION FACTOR-XI AS A NEWLY RECOGNIZED FEATURE OF NOONAN SYNDROME

被引:32
作者
KITCHENS, CS
ALEXANDER, JA
机构
[1] UNIV FLORIDA, DEPT MED, DIV HEMATOL, GAINESVILLE, FL 32611 USA
[2] UNIV FLORIDA, DEPT SURG, DIV CARDIOTHORAC SURG, GAINESVILLE, FL 32611 USA
关键词
D O I
10.1016/S0022-3476(83)80525-3
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:224 / 227
页数:4
相关论文
共 21 条
[1]   NOONAN SYNDROME - FAMILY STUDY [J].
BOLTON, MR ;
PUGH, DM ;
MATTIOLI, LF ;
DUNN, MI ;
SCHIMKE, RN .
ANNALS OF INTERNAL MEDICINE, 1974, 80 (05) :626-629
[2]   PULMONARY STENOSIS IN PATIENTS WITH TURNER PHENOTYPE IN MALE [J].
CELERMAJER, JM ;
BOWDLER, JD ;
COHEN, DH .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1968, 116 (04) :351-+
[3]  
CHAR F, 1972, Birth Defects Original Article Series, V8, P110
[4]   PULMONARY LYMPHANGIECTASIS IN NOONAN SYNDROME [J].
HERNANDEZ, RJ ;
STERN, AM ;
ROSENTHAL, A .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1980, 134 (01) :75-80
[5]   CARDIAC SURGERY IN PATIENTS WITH PLASMA THROMBOPLASTIN ANTECEDENT (PTA) DEFICIENCY [J].
HILGARTNER, M ;
ENGLE, MA ;
REDO, SF .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1965, 49 (06) :974-+
[6]   FACTOR-XIII [J].
KITCHENS, CS ;
NEWCOMB, TF .
MEDICINE, 1979, 58 (06) :413-429
[7]  
MCKUSICK VA, 1975, MENDELIAN INHERITANC, P235
[8]   NOONAN SYNDROME IN AN ADULT FAMILY PRESENTING WITH CHRONIC LYMPHEDEMA [J].
MILLER, M ;
MOTULSKY, AC .
AMERICAN JOURNAL OF MEDICINE, 1978, 65 (02) :379-383
[9]   HYPERTELORISM WITH TURNER PHENOTYPE - A NEW SYNDROME WITH ASSOCIATED CONGENITAL HEART DISEASE [J].
NOONAN, JA .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1968, 116 (04) :373-&
[10]  
NOONAN JA, 1963, J PEDIATR-US, V63, P468