THE MECKEL SYNDROME IN THE HUTTERITES

被引：24

作者：

SCHURIG, V

BOWEN, P

HARLEY, F

SCHIFF, D

机构：

[1] UNIV ALBERTA,DEPT PEDIAT,DIV NEPHROL,EDMONTON T6G 2G3,ALBERTA,CANADA

[2] UNIV ALBERTA,DEPT PEDIAT,DIV NEONATOL,EDMONTON T6G 2G3,ALBERTA,CANADA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1980年 / 5卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320050408

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：373 / 381

页数：9

共 18 条

[1] CASUISTIC REPORT ON GRUBER OR MECKEL SYNDROME [J].

ALTMANN, P ;

WAGENBICHLER, P ;

SCHALLER, A .

HUMAN GENETICS, 1977, 38 (03) :357-362

[2]

BERNSTEIN J, 1973, PERSPECTIVES PEDIATR, P133

[3]

CHEMKE J, 1977, CLIN GENET, V11, P285

[4]

EATON JOSEPH W., 1953, HUMAN BIOL, V25, P206

[5]

FITCH N, 1973, CLIN GENET, V4, P33

[6]

FRASER FC, 1978, 29TH ANN M AM SOC HU

[7]

FRIED K, 1974, CLIN GENET, V5, P46

[8]

Hostetler J., 1974, HUTTERITE SOC

[9] BOWEN-CONRADI SYNDROME - HIGHLY LETHAL AUTOSOMAL RECESSIVE SYNDROME OF MICROCEPHALY, MICROGNATHIA, LOW BIRTH-WEIGHT, AND JOINT DEFORMITIES [J].

HUNTER, AGW ;

WOERNER, SJ ;

MONTALVOHICKS, LDC ;

FOWLOW, SB ;

HASLAM, RHA ;

METCALF, PJ ;

LOWRY, RB .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1979, 3 (03) :269-279

[10]

MACRAE DW, 1972, ARCH OPHTHALMOL-CHIC, V88, P106

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