PRENATAL-DIAGNOSIS OF MECKEL SYNDROME - CASE-REPORTS AND LITERATURE-REVIEW

被引：12

作者：

JOHNSON, VP

HOLZWARTH, DR

机构：

[1] UNIV S DAKOTA,SCH MED,DEPT OBSTET & GYNECOL,VERMILLION,SD 57069

[2] UNIV S DAKOTA,SCH MED,DEPT PEDIAT,VERMILLION,SD 57069

[3] UNIV S DAKOTA,SCH MED,DEPT LAB MED,VERMILLION,SD 57069

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1984年 / 18卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320180416

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：699 / 711

页数：13

共 23 条

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[4]

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[7]

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[8]

FRYNS JP, 1980, J GENET HUM, V28, P89

[9] AMNIOTIC-FLUID PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN (SP1) IN MECKELS SYNDROME - A NEW TEST FOR PRENATAL-DIAGNOSIS [J].

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SEPPALA, M .

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[10] ETIOLOGIC HETEROGENEITY OF NEURAL-TUBE DEFECTS [J].

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