TRISOMY 11P15 AND BECKWITH-WIEDEMANN SYNDROME - A REPORT OF 2 CASES

被引：135

作者：

TURLEAU, C

DEGROUCHY, J

CHAVINCOLIN, F

MARTELLI, H

VOYER, M

CHARLAS, R

机构：

[1] HOP NECKER,CNRS,ER 149,F-75743 PARIS 15,FRANCE

[2] HOP NECKER,CHIRURG INFANTILE CLIN,F-75730 PARIS 15,FRANCE

[3] HOP NECKER,INSERM,U173,F-75730 PARIS 15,FRANCE

[4] INST PUERICULTURE,F-75014 PARIS,FRANCE

来源：

HUMAN GENETICS | 1984年 / 67卷 / 02期

关键词：

D O I：

10.1007/BF00273006

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：219 / 221

页数：3

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[2]

COHEN MM, 1979, BIRTH DEFECTS COMPEN

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[4]

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[5]

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[6]

MCKUSICK VA, 1983, MENDELIAN INHERITANC, P1378

[7] COMPLETE AND INCOMPLETE FORMS OF BECKWITH-WIEDEMANN SYNDROME - THEIR ONCOGENIC POTENTIAL [J].

SOTELOAVILA, C ;

GONZALEZCRUSSI, F ;

FOWLER, JW .

JOURNAL OF PEDIATRICS, 1980, 96 (01) :47-50

[8] ABNORMALITY OF CHROMOSOME-11 IN PATIENTS WITH FEATURES OF BECKWITH-WIEDEMANN SYNDROME [J].

WAZIRI, M ;

PATIL, SR ;

HANSON, JW ;

BARTLEY, JA .

JOURNAL OF PEDIATRICS, 1983, 102 (06) :873-876

[9]

WIEDEMANN H. R., 1964, J GENET HUM, V13, P223

[10]

1984, CYTOGENET CELL GENET, V37, P1

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