SURVIVAL AND SPECTRUM OF ANOMALIES IN THE MECKEL SYNDROME

被引：32

作者：

LOWRY, RB

HILL, RH

TISCHLER, B

机构：

[1] UNIV CALGARY,DEPT PEDIAT,CALGARY T2N 1N4,ALBERTA,CANADA

[2] UNIV BRITISH COLUMBIA,DEPT PAEDIAT,VANCOUVER V6T 1W5,BC,CANADA

[3] UNIV BRITISH COLUMBIA,DEPT MED GENET,VANCOUVER V6T 1W5,BC,CANADA

[4] WOODLANDS,NEW WESTMINSTER,BC,CANADA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1983年 / 14卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320140303

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：417 / 421

页数：5

共 9 条

[1]

CASSIDY SB, 1977, ANN GENET-PARIS, V20, P277

[2] SPECTRUM OF ANOMALIES IN THE MECKEL SYNDROME, OR - MAYBE THERE IS A MALFORMATION SYNDROME WITH AT LEAST ONE CONSTANT ANOMALY [J].

FRASER, FC ;

LYTWYN, A .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1981, 9 (01) :67-73

[3] SMITH-LEMLI-OPITZ SYNDROME - REVIEW AND REPORT OF 2 AFFECTED SIBLINGS [J].

JOHNSON, VP .

ZEITSCHRIFT FUR KINDERHEILKUNDE, 1975, 119 (04) :221-234

[4] BORDERLINE NORMAL INTELLIGENCE IN THE SMITH-LEMLI-OPITZ (RSH) SYNDROME [J].

LOWRY, RB ;

YONG, SL .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 5 (02) :137-143

[5]

MALPUECH G, 1979, J GENET HUM, V27, P167

[6]

MECKE S, 1971, ANN GENET-PARIS, V14, P97

[7]

OPITZ J M, 1969, Birth Defects Original Article Series, V5, P167

[8] THE MECKEL SYNDROME IN THE HUTTERITES [J].

SCHURIG, V ;

BOWEN, P ;

HARLEY, F ;

SCHIFF, D .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 5 (04) :373-381

[9]

SELLER MJ, 1981, CLIN GENET, V20, P74

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