NEU-LAXOVA SYNDROME AND CAD COMPLEX - COMMENTS

被引：35

作者：

SCOTT, CI

LOURO, JM

LAURENCE, KM

TOLAROVA, M

HALL, JG

REED, S

CURRY, CJR

机构：

[1] UNIV TEXAS, HLTH SCI CTR, DEPT PEDIAT, SAN ANTONIO, TX 78284 USA

[2] UNIV WALES WELSH NATL SCH MED, DEPT CHILD HLTH, CHILD HLTH LAB, CARDIFF CF4 4XN, S GLAMORGAN, WALES

[3] CZECHOSLOVAK ACAD SCI, INST EXPTL MED, DEPT BIRTH DEFECTS, GENET UNIT, PRAGUE, CZECHOSLOVAKIA

[4] VALLEY CHILDRENS HOSP & GUIDANCE CLIN, GENET & PRENATAL DETECT UNIT, FRESNO, CA USA

[5] UNIV WASHINGTON, CHILDRENS ORTHOPED HOSP, DEPT PEDIAT, SEATTLE, WA 98195 USA

[6] UNIV WASHINGTON, CHILDRENS ORTHOPED HOSP, DEPT MED MED GENET, SEATTLE, WA 98195 USA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1981年 / 9卷 / 02期

关键词：

D O I：

10.1002/ajmg.1320090211

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：165 / 175

页数：11

共 7 条

[1]

DEMYER W, 1964, PEDIATRICS, V34, P256

[2]

LAXOVA R, 1972, J MENT DEFIC RES, V16, P139

[3] NEU-LAXOVA SYNDROME - DISTINCT ENTITY [J].

LAZJUK, GI ;

LURIE, IW ;

OSTROWSKAJA, TI ;

CHERSTVOY, ED ;

KIRILLOVA, IA ;

NEDZVED, MK ;

USOEV, SS .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1979, 3 (03) :261-267

[4] APROSENCEPHALY-ATELENCEPHALY AND THE APROSENCEPHALY (XK) SYNDROME [J].

LURIE, IW ;

NEDZVED, MK ;

LAZJUK, GI ;

KIRILLOVA, IA ;

CHERSTVOY, ED .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1979, 3 (03) :303-309

[5]

NEU RL, 1971, PEDIATRICS, V47, P610

[6]

Povysilova V, 1976, Cesk Pediatr, V31, P190

[7] CEREBROARTHRODIGITAL SYNDROME - NEWLY RECOGNIZED FORMAL GENESIS SYNDROME IN 3 PATIENTS WITH APPARENT ARTHROMYODYSPLASIA AND SACRAL AGENESIS, BRAIN MALFORMATION AND DIGITAL HYPOPLASIA [J].

SPRANGER, JW ;

SCHINZEL, A ;

MYERS, T ;

RYAN, J ;

GIEDION, A ;

OPITZ, JM .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 5 (01) :13-24

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