DERMATOGLYPHICS AND SYNDROMES

被引：64

作者：

PREUS, M

FRASER, FC

机构：

[1] MONTREAL CHILDRENS HOSP, DEPT MED GENET, MONTREAL 108, QUEBEC, CANADA

[2] MCGILL UNIV, MONTREAL, QUEBEC, CANADA

来源：

AMERICAN JOURNAL OF DISEASES OF CHILDREN | 1972年 / 124卷 / 06期

关键词：

D O I：

10.1001/archpedi.1972.02110180135022

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：933 / 943

页数：11

共 100 条

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[2] UNUSUAL DERMATOGLYPHIC FINDINGS ASSOCIATED WITH RUBELLA EMBRYOPATHY [J].

ACHS, R ;

HARPER, RG ;

SIEGEL, M .

NEW ENGLAND JOURNAL OF MEDICINE, 1966, 274 (03) :148-&

[3]

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[4]

ANDERMANN E, 1966, THESIS MCGILL U

[5] HUMAN CHROMOSOMAL DELETION . 2 PATIENTS WITH 4P-SYNDROME [J].

ARIAS, D ;

PASSARGE, E ;

ENGLE, MA ;

GERMAN, J .

JOURNAL OF PEDIATRICS, 1970, 76 (01) :82-+

[6]

BECKMAN L, 1962, ACTA GENET STAT MED, V12, P20

[7]

Berg J M, 1968, J Ment Defic Res, V12, P307

[8]

BERG JM, 1966, J MENT DEFIC RES, V10, P204

[9]

BERG JM, 1970, DELANGE SYNDROME

[10]

BERKA L, 1971, CAN MED ASSOC J, V105, P476

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