NEUROFIBROMATOSIS WITH FULLY EXPRESSED NOONAN SYNDROME

被引：29

作者：

ABUELO, DN ^{[1
]}

MERYASH, DL ^{[1
]}

机构：

[1] BROWN UNIV,RHODE ISL HOSP,PROGRAM MED,DEPT PEDIAT,CTR CHILD DEV,PROVIDENCE,RI 02902

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1988年 / 29卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320290426

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：937 / 941

页数：5

共 13 条

[1] NOONAN SYNDROME
ALLANSON, JE
[J]. JOURNAL OF MEDICAL GENETICS, 1987, 24 (01) : 9 - 13
[2] NOONAN PHENOTYPE ASSOCIATED WITH NEUROFIBROMATOSIS
ALLANSON, JE
HALL, JG
VANALLEN, MI
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03): : 457 - 462
[3] CONGENITAL LID PTOSIS ASSOCIATED WITH NEUROFIBROMATOSIS
HALL, BD
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 25 (03): : 595 - 597
[4] HALL JG, 1983, P GREENWOOD GENET CT, V2, P114
[5] A DISTINCTIVE FACIAL APPEARANCE IN NEUROFIBROMATOSIS VONRECKLINGHAUSEN
KAPLAN, P
ROSENBLATT, B
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03): : 463 - 470
[6] EVIDENCE THAT THE NEUROFIBROMATOSIS-NOONAN SYNDROME IS A VARIANT OF VON RECKLINGHAUSEN NEUROFIBROMATOSIS
MEINECKE, P
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 26 (03): : 741 - 745
[7] THE NEUROFIBROMATOSIS-NOONAN SYNDROME
MENDEZ, HMM
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03): : 471 - 476
[8] MENDEZ HMM, 1984, P GREENWOOD GENET CT, V3, P158
[9] MENDEZ HMM, 1983, DW SMITH MORPHOGENES, P99
[10] NOONAN JA, 1963, J PEDIATR-US, V63, P468