HUMAN CHROMOSOMAL DEFICIENCY - 4P-SYNDROME

被引：20

作者：

PASSARGE, E

ALTROGGE, HC

RUDIGER, RA

机构：

来源：

HUMANGENETIK | 1970年 / 10卷 / 01期

关键词：

D O I：

10.1007/BF00297640

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：51 / &

共 23 条

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[4]

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[5]

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[6]

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[7]

HIRSCHHORN K, 1965, HUMANGENETIK, V1, P479

[8] SCREENING FOR MINUTE DELETIONS IN PATIENTS WITH SUSPECTED CRI-DU-CHAT SYNDROME AND APPARENTLY NORMAL KARYOTYPE [J].

HOEHN, H ;

ENGEL, W .

HUMANGENETIK, 1969, 8 (02) :105-&

[9]

JUBERG R C, 1969, Journal of Medical Genetics, V6, P314, DOI 10.1136/jmg.6.3.314

[10]

LEAO JC, 1967, JAMA-J AM MED ASSOC, V202, P132

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