THE WIEDEMANN-RAUTENSTRAUCH OR NEONATAL PROGEROID SYNDROME - REPORT OF A PATIENT WITH CONSANGUINEOUS PARENTS

被引：49

作者：

DEVOS, EA

LEROY, JG

FRIJNS, JP

VANDENBERGHE, H

机构：

[1] ANTWERP UNIV, SCH MED, DIV MED GENET, B-2610 WILRIJK, BELGIUM

[2] H HART HOSP, DIV PEDIAT, ROESELARE, BELGIUM

[3] CATHOLIC UNIV LEUVEN, DEPT HUMAN BIOL, DIV HUMAN GENET, B-3000 LOUVAIN, BELGIUM

来源：

关键词：

D O I：

10.1007/BF00442991

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：245 / 248

页数：4

共 7 条

DEBUSK, FL .

[2]

Gorlin RJ., 1976, SYNDROMES HEAD NECK, V2nd

[3]

LEROY JG, 1978, BIRTH DEFECTS OAS, V14, P374

RAUTENSTRAUCH, T ;

SNIGULA, F ;

KRIEG, T ;

GAY, S ;

MULLER, PK .

[5]

Seip M, 1971, Ergeb Inn Med Kinderheilkd, V31, P59

[6] UNIDENTIFIED NEONATAL PROGEROID SYNDROME - FOLLOW-UP REPORT [J].

WIEDEMANN, HR .

[7]

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