PRENATAL ULTRASOUND DIAGNOSIS OF MACROGLOSSIA IN THE WIEDEMANN-BECKWITH SYNDROME

被引：18
作者：
COBELLIS, G
IANNOTO, P
STABILE, M
LONARDO, F
DELLABRUNA, M
CALIENDO, E
VENTRUTO, V
机构：
[1] OSPED CARDARELLI,SERV GENET MED,I-80131 NAPOLI,ITALY
[2] OSPED RIUNITI S GIOVANNI DIO & RUGGI DARAGONA,DIV NEONATOL,SALERNO,ITALY
来源：
PRENATAL DIAGNOSIS | 1988年 / 8卷 / 01期
关键词：
D O I：
10.1002/pd.1970080112
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：79 / 81
页数：3
相关论文
共 5 条
  • [1] McKusick V. A., 1986, MENDELIAN INHERITANC
  • [2] WIEDEMANN-BECKWITH SYNDROME - PRESENTATION OF CLINICAL AND CYTOGENETIC DATA ON 22 NEW CASES AND REVIEW OF THE LITERATURE
    PETTENATI, MJ
    HAINES, JL
    HIGGINS, RR
    WAPPNER, RS
    PALMER, CG
    WEAVER, DD
    [J]. HUMAN GENETICS, 1986, 74 (02) : 143 - 154
  • [3] SHAPIRO LR, 1982, BIRTH DEFECTS-ORIG, V18, P203
  • [4] INUTERO DIAGNOSIS OF BECKWITH-WIEDEMANN SYNDROME BY ULTRASOUND
    WEINSTEIN, L
    ANDERSON, C
    [J]. RADIOLOGY, 1980, 134 (02) : 474 - 474
  • [5] PRENATAL-DIAGNOSIS OF THE BECKWITH-WIEDEMANN SYNDROME
    WINTER, SC
    CURRY, CJR
    SMITH, JC
    KASSEL, S
    MILLER, L
    ANDREA, J
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 24 (01): : 137 - 141
1