NAGER ACROFACIAL DYSOSTOSIS - AUTOSOMAL DOMINANT INHERITANCE IN MILD TO MODERATELY AFFECTED MOTHER AND LETHALLY AFFECTED PHOCOMELIC SON

被引：25

作者：

HALL, BD

机构：

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1989年 / 33卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320330321

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：394 / 397

页数：4

共 6 条

[1]

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[3] NAGER ACROFACIAL DYSOSTOSIS - EVIDENCE FOR APPARENT HETEROGENEITY [J].

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[4] DIFFERENTIAL-DIAGNOSIS OF NAGER ACROFACIAL DYSOSTOSIS SYNDROME - REPORT OF 4 PATIENTS WITH NAGER SYNDROME AND DISCUSSION OF OTHER RELATED SYNDROMES [J].

HALAL, F ;

HERRMANN, J ;

PALLISTER, PD ;

OPITZ, JM ;

DESGRANGES, MF ;

GRENIER, G .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 14 (02) :209-224

[5] THE NAGER SYNDROME [J].

HECHT, JT ;

IMMKEN, LL ;

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SCOTT, CI .

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[6]

Lowry R B, 1977, Birth Defects Orig Artic Ser, V13, P195

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