A CHROMOSOMAL BREAKPOINT THAT SEPARATES THE ESTERASE-D AND RETINOBLASTOMA PREDISPOSITION LOCI IN A PATIENT WITH DEL(13)(Q14Q31)

被引：17

作者：

COWELL, JK

HUNGERFORD, J

RUTLAND, P

JAY, M

机构：

[1] ST BARTHOLOMEWS HOSP,DEPT OPHTHALMOL,LONDON EC1A 7BE,ENGLAND

[2] MOORFIELDS EYE HOSP,DEPT CLIN OPHTHALMOL,LONDON WC1V 7AN,ENGLAND

[3] INST CHILD HLTH,PAEDIAT GENET MOTHERCARE UNIT,LONDON WC1N 1EH,ENGLAND

来源：

关键词：

D O I：

10.1016/0165-4608(87)90256-1

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

引用

页码：27 / 31

页数：5

共 10 条

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[3] COWELL JK, 1985, CANCER SURV, V3, P573
[4] ESTERASE-D - NEW HUMAN POLYMORPHISM
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[5] GENE FOR HEREDITARY RETINOBLASTOMA ASSIGNED TO HUMAN CHROMOSOME-13 BY LINKAGE TO ESTERASE-D
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[8] CYTOGENETIC FORMS OF RETINOBLASTOMA - THEIR INCIDENCE IN A SURVEY OF 66 PATIENTS
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[J]. CANCER GENETICS AND CYTOGENETICS, 1985, 16 (04) : 321 - 334
[9] VOGEL F, 1979, HUM GENET, V52, P1
[10] RETINOBLASTOMA AND SUBBAND DELETION OF CHROMOSOME-13
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[J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1978, 132 (02): : 161 - 163