FAMILIAL RETINOBLASTOMA (MOTHER AND SON) WITH 13Q14 DELETION

被引：16

作者：

FUKUSHIMA, Y

KUROKI, Y

ITO, T

KONDO, I

NISHIGAKI, I

机构：

[1] KANAGAWA CHILDRENS MED CTR,DIV MED GENET,YOKOHAMA 232,JAPAN

[2] KANAGAWA CHILDRENS MED CTR,DIV OPHTHALMOL,YOKOHAMA 232,JAPAN

[3] UNIV TSUKUBA,INST BASIC MED SCI,DEPT HUMAN GENET,SAKURA,IBARAKI 305,JAPAN

来源：

HUMAN GENETICS | 1987年 / 77卷 / 02期

关键词：

D O I：

10.1007/BF00272373

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：104 / 107

页数：4

共 16 条

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[5] DELETION OF 13Q IN 2 PATIENTS WITH RETINOBLASTOMA, ONE PROBABLY DUE TO 13Q- MOSAICISM IN THE MOTHER [J].

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[6] A RECOGNIZABLE PATTERN OF THE MIDFACE OF RETINOBLASTOMA PATIENTS WITH INTERSTITIAL DELETION OF 13Q [J].

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HUMAN GENETICS, 1983, 64 (02) :160-162

[7] IS THE INTERSTITIAL DELETION OF 13Q IN RETINOBLASTOMA PATIENTS NOT TRANSMISSIBLE [J].

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KOMATSU, M ;

MINODA, K .

HUMAN GENETICS, 1983, 64 (02) :205-205

[8] QUANTITATIVE VARIATIONS IN POLYMORPHIC TYPES OF HUMAN RED-CELL ESTERASE-D [J].

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[9]

NOEL B, 1976, CLIN GENET, V9, P593

[10]

RICCARDI VM, 1979, CLIN GENET, V15, P332

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