THE NEUROFIBROMATOSIS-NOONAN SYNDROME - COMMENT

被引：73

作者：

OPITZ, JM ^{[1
]}

WEAVER, DD ^{[1
]}

机构：

[1] INDIANA UNIV,MED CTR,DEPT MED GENET,INDIANAPOLIS,IN 46204

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1985年 / 21卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320210310

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：477 / 490

页数：14

共 18 条

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HALL, JG
VANALLEN, MI
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03): : 457 - 462
[3] CAREY J, COMMUNICATION
[4] FEGELER F, 1952, Dtsch Z Nervenheilkd, V168, P427
[5] HALL JG, 1983, P GREENWOOD GENET CT, V2, P114
[6] Harbitz F, 1916, BEITR PATHOL ANAT AL, V62, P503
[7] DAS MORGAGNI-TURNER-SYNDROM
HENI, F
[J]. KLINISCHE WOCHENSCHRIFT, 1951, 29 (5-6): : 75 - 80
[8] NOONANS SYNDROME - A CASE WITH ELEVATED SERUM ALKALINE PHOSPHATASE LEVELS AND MALIGNANT SCHWANNOMA OF LEFT FOREARM
KAPLAN, MS
OPITZ, JM
GOSSET, FR
[J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1968, 116 (04): : 359 - &
[9] A DISTINCTIVE FACIAL APPEARANCE IN NEUROFIBROMATOSIS VONRECKLINGHAUSEN
KAPLAN, P
ROSENBLATT, B
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03): : 463 - 470
[10] THE NEUROFIBROMATOSIS-NOONAN SYNDROME
MENDEZ, HMM
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03): : 471 - 476