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

页码：79 / 81

页数：3

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 [J].

PETTENATI, MJ ;

HAINES, JL ;

HIGGINS, RR ;

WAPPNER, RS ;

PALMER, CG ;

WEAVER, DD .

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 [J].

WEINSTEIN, L ;

ANDERSON, C .

RADIOLOGY, 1980, 134 (02) :474-474

[5] PRENATAL-DIAGNOSIS OF THE BECKWITH-WIEDEMANN SYNDROME [J].

WINTER, SC ;

CURRY, CJR ;

SMITH, JC ;

KASSEL, S ;

MILLER, L ;

ANDREA, J .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 24 (01) :137-141

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