4P- PHENOTYPE IN AN INFANT WITH T(4P-19P OR Q+)MAT TRANSLOCATION

被引：17

作者：

NEU, RL ^{[1
]}

SHOTT, RJ ^{[1
]}

GARDNER, LI ^{[1
]}

机构：

[1] SUNY, UPSTATE MED CTR,DEPT PEDIAT, GENET & ENDOCRINE UNIT,750 E ADAMS ST, SYRACUSE, NY 13210 USA

来源：

AMERICAN JOURNAL OF DISEASES OF CHILDREN | 1975年 / 129卷 / 03期

关键词：

D O I：

10.1001/archpedi.1975.02120400063015

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：363 / 365

页数：3

共 8 条

[1]

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[2]

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[4] 4P- SYNDROME - CLINICALLY RECOGNIZABLE CHROMOSOMAL DELETION SYNDROME [J].

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AASE, JM ;

ASPER, AC ;

SMITH, DW .

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[5] B-F CHROMOSOME TRANSLOCATION ASSOCIATED WITH FATHER-CHILD INCOMPATIBILITY WITHIN GE-SYSTEM [J].

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MIKKELSEN, M .

HUMAN HEREDITY, 1969, 19 (03) :283-+

[6]

Lejeune J, 1965, Ann Genet, V8, P21

[7] CLINICAL MANIFESTATIONS AND CYTOGENETIC OBSERVATIONS OF 7 CASES AFFECTED BY CRI-DU-CHAT SYNDROME [J].

MENNICKEN, U ;

PFEIFFER, RA ;

PUYN, U ;

WORBES, H ;

WAGENER, A .

ZEITSCHRIFT FUR KINDERHEILKUNDE, 1968, 104 (03) :230-+

[8] CRI-DU-CHAT-SYNDROM WITH TRANSLOCATION [J].

WOLF, U ;

REINWEIN, H ;

KLOSE, J .

HUMANGENETIK, 1966, 2 (01) :63-63

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