NOONAN SYNDROME

被引:309
作者
ALLANSON, JE
机构
关键词
D O I
10.1136/jmg.24.1.9
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
引用
收藏
页码:9 / 13
页数:5
相关论文
共 47 条
[1]
NOONAN SYNDROME - THE CHANGING PHENOTYPE [J].
ALLANSON, JE ;
HALL, JG ;
HUGHES, HE ;
PREUS, M ;
WITT, RD .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03) :507-514
[2]
NOONAN PHENOTYPE ASSOCIATED WITH NEUROFIBROMATOSIS [J].
ALLANSON, JE ;
HALL, JG ;
VANALLEN, MI .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03) :457-462
[3]
ALLANSON JE, UNPUB COLLABORATIVE
[4]
BALL MJ, 1982, J NEUROL NEUROSUR PS, V45, P753
[5]
PHEOCHROMOCYTOMA AND HYPORESPONSIVENESS TO THYROTROPHIN IN A 46 XY MALE WITH FEATURES OF TURNER PHENOTYPE [J].
BECKER, CE ;
ROSEN, SW ;
ENGELMAN, K .
ANNALS OF INTERNAL MEDICINE, 1969, 70 (02) :325-+
[6]
Berberich M S, 1976, Birth Defects Orig Artic Ser, V12, P181
[7]
CHAR F, 1972, Birth Defects Original Article Series, V8, P110
[8]
CHAVESCARBALLO E, 1966, MAYO CLIN PROC, V41, P843
[9]
NECK WEB AND CONGENITAL HEART-DEFECTS - A PATHOGENIC ASSOCIATION IN 45 X-O TURNER SYNDROME [J].
CLARK, EB .
TERATOLOGY, 1984, 29 (03) :355-361
[10]
CLARK EB, 1985, P GREENWOOD GENET CE, V4, P80