CATCHING A BREAK ON 22

被引：22

作者：

GLOVER, TW ^{[1
]}

机构：

[1] UNIV MICHIGAN,DEPT HUMAN GENET,ANN ARBOR,MI 48109

来源：

NATURE GENETICS | 1995年 / 10卷 / 03期

关键词：

D O I：

10.1038/ng0795-257

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：257 / 258

页数：2

共 19 条

[1] ISOLATION OF A ZINC-FINGER GENE CONSISTENTLY DELETED IN DIGEORGE-SYNDROME [J].

AUBRY, M ;

DEMCZUK, S ;

DESMAZE, C ;

AIKEM, M ;

AURIAS, A ;

JULIEN, JP ;

ROULEAU, GA .

HUMAN MOLECULAR GENETICS, 1993, 2 (10) :1583-1587

[2] DIGEORGE SYNDROME AND 22Q11 REARRANGEMENTS [J].

AUGUSSEAU, S ;

JOUK, S ;

JALBERT, P ;

PRIEUR, M .

HUMAN GENETICS, 1986, 74 (02) :206-206

[3] CLONING A BALANCED TRANSLOCATION ASSOCIATED WITH DIGEORGE-SYNDROME AND IDENTIFICATION OF A DISRUPTED CANDIDATE GENE [J].

BUDARF, ML ;

COLLINS, J ;

GONG, WL ;

ROE, B ;

WANG, ZL ;

BAILEY, LC ;

SELLINGER, B ;

MICHAUD, D ;

DRISCOLL, DA ;

EMANUEL, BS .

NATURE GENETICS, 1995, 10 (03) :269-278

[4] CONOTRUNCAL ANOMALY FACE SYNDROME IS ASSOCIATED WITH A DELETION WITHIN CHROMOSOME-22Q11 [J].

BURN, J ;

TAKAO, A ;

WILSON, D ;

CROSS, I ;

MOMMA, K ;

WADEY, R ;

SCAMBLER, P ;

GOODSHIP, J .

JOURNAL OF MEDICAL GENETICS, 1993, 30 (10) :822-824

[5] A DELETION IN CHROMOSOME-22 CAN CAUSE DIGEORGE SYNDROME [J].

DELACHAPELLE, A ;

HERVA, R ;

KOIVISTO, M ;

AULA, P .

HUMAN GENETICS, 1981, 57 (03) :253-256

[6]

DEMCZUK S, 1995, HUM MOL GENET, V4, P451

[7]

DiGeorge A. M., 1965, J PEDIATR, V67, P907, DOI DOI 10.1016/S0022-3476(65)81796-6)

[8]

DRIACOLL DA, 1993, J MED GENET, V30, P822

[9] CAMPOMELIC DYSPLASIA AND AUTOSOMAL SEX REVERSAL CAUSED BY MUTATIONS IN AN SRY-RELATED GENE [J].

FOSTER, JW ;

DOMINGUEZSTEGLICH, MA ;

GUIOLI, S ;

KWOK, C ;

WELLER, PA ;

STEVANOVIC, M ;

WEISSENBACH, J ;

MANSOUR, S ;

YOUNG, ID ;

GOODFELLOW, PN ;

BROOK, JD ;

SCHAFER, AJ .

NATURE, 1994, 372 (6506) :525-530

[10] MICRODELETIONS OF CHROMOSOMAL REGION 22Q11 IN PATIENTS WITH CONGENITAL CONOTRUNCAL CARDIAC DEFECTS [J].

GOLDMUNTZ, E ;

DRISCOLL, D ;

BUDARF, ML ;

ZACKAI, EH ;

MCDONALDMCGINN, DM ;

BIEGEL, JA ;

EMANUEL, BS .

JOURNAL OF MEDICAL GENETICS, 1993, 30 (10) :807-812

← 1 2 →