ANTENATAL DIAGNOSIS OF DIGEORGE SYNDROME

被引：17

作者：

DRISCOLL, DA

BUDARF, ML

EMANUEL, BS

机构：

[1] UNIV PENN,SCH MED,DEPT PEDIAT,PHILADELPHIA,PA 19104

[2] UNIV PENN,SCH MED,DEPT HUMAN GENET,PHILADELPHIA,PA 19104

来源：

LANCET | 1991年 / 338卷 / 8779期

关键词：

D O I：

10.1016/0140-6736(91)92264-3

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1390 / 1391

页数：2

共 9 条

[1] PREDICTION OF PERSISTENT IMMUNODEFICIENCY IN THE DIGEORGE ANOMALY [J].

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HERROD, H ;

ANDERSON, S ;

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HONG, R .

JOURNAL OF PEDIATRICS, 1989, 115 (03) :391-396

[2] FAILURE OF FETAL KARYOTYPING AND DIAGNOSIS OF COMPLETE DIGEORGE SYNDROME [J].

CATHERINE, N ;

GIOVANGRANDI, Y ;

BAZIN, A ;

DAFFOS, F ;

FORESTIER, F .

LANCET, 1991, 337 (8736) :299-300

[3] SPECTRUM OF THE DIGEORGE SYNDROME [J].

CONLEY, ME ;

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MANCER, JFK ;

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[4]

DRISCOLL DA, 1991, AM J HUM GENET, V49, pA86

[5]

DRISCOLL DA, 1990, AM J HUM GENET, V47, pA215

[6]

GREENBERG F, 1988, AM J HUM GENET, V43, P605

[7]

KUWANO A, 1991, AM J HUM GENET, V49, P707

[8] INTERSTITIAL DELETION OF CHROMOSOME-22 IN A PATIENT WITH THE DIGEORGE MALFORMATION SEQUENCE [J].

MASCARELLO, JT ;

BASTIAN, JF ;

JONES, MC .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 32 (01) :112-114

[9] MICRODELETIONS WITHIN 22Q11 ASSOCIATED WITH SPORADIC AND FAMILIAL DIGEORGE SYNDROME [J].

SCAMBLER, PJ ;

CAREY, AH ;

WYSE, RKH ;

ROACH, S ;

DUMANSKI, JP ;

NORDENSKJOLD, M ;

WILLIAMSON, R .

GENOMICS, 1991, 10 (01) :201-206

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