CENTROMERIC INSTABILITY OF CHROMOSOME-1 AND CHROMOSOME-16 WITH VARIABLE IMMUNE-DEFICIENCY - A NEW SYNDROME

被引：0

作者：

HOWARD, PJ ^{[1
]}

LEWIS, IJ ^{[1
]}

HARRIS, F ^{[1
]}

WALKER, S ^{[1
]}

机构：

[1] ALDER HEY CHILDRENS HOSP,DEPT CHILD HLTH,LIVERPOOL L12 2AP,MERSEYSIDE,ENGLAND

来源：

CLINICAL GENETICS | 1985年 / 27卷 / 05期

关键词：

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：501 / 505

页数：5

共 4 条

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FRYNS, JP ;

AZOU, M ;

JAEKEN, J ;

EGGERMONT, E ;

PEDERSEN, JC ;

VANDENBERGHE, H .

HUMAN GENETICS, 1981, 57 (01) :108-110

[2]

HULTEN M, 1978, CLIN GENET, V14, P294

[3] MULTIBRANCHED CHROMOSOME-1, CHROMOSOME-9, AND CHROMOSOME-16 IN A PATIENT WITH COMBINED IGA AND IGE DEFICIENCY [J].

TIEPOLO, L ;

MARASCHIO, P ;

GIMELLI, G ;

CUOCO, C ;

GARGANI, GF ;

ROMANO, C .

HUMAN GENETICS, 1979, 51 (02) :127-137

[4] A NEW CHROMOSOMAL INSTABILITY DISORDER - THE NIJMEGEN BREAKAGE SYNDROME [J].

WEEMAES, CMR ;

HUSTINX, TWJ ;

SCHERES, JMJC ;

VANMUNSTER, PJJ ;

BAKKEREN, JAJM ;

TAALMAN, RDFM .

ACTA PAEDIATRICA SCANDINAVICA, 1981, 70 (04) :557-564

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