Prenatal diagnosis of mosaic 22q11.2 microdeletion

被引：12

作者：

Chen, CP ^{[1
]}

Chern, SR

Lee, CC

Lin, SP

Chang, TY

Wang, WS

机构：

[1] Mackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan

[2] Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan

[3] Natl Yang Ming Univ, Coll Nursing, Taipei 112, Taiwan

[4] Mackay Mem Hosp, Dept Pediat, Taipei, Taiwan

来源：

PRENATAL DIAGNOSIS | 2004年 / 24卷 / 08期

关键词：

D O I：

10.1002/pd.917

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：660 / 662

页数：3

共 24 条

[21] RECURRENCE OF DIGEORGE-SYNDROME - PRENATAL DETECTION BY FISH OF A MOLECULAR 22Q11 DELETION [J].

VANHEMEL, JO ;

SCHAAP, C ;

VANOPSTAL, D ;

MULDER, MP ;

NIERMEIJER, MF ;

MEIJERS, JHC .

JOURNAL OF MEDICAL GENETICS, 1995, 32 (08) :657-658

[22]

Vantrappen G, 1999, GENET COUNSEL, V10, P3

[23] 22q11 deletions in fetuses with malformations of the outflow tracts or interruption of the aortic arch: impact of additional ultrasound signs [J].

Volpe, P ;

Marasini, M ;

Caruso, G ;

Marzullo, A ;

Buonadonna, AL ;

Arciprete, P ;

Di Paolo, S ;

Volpe, G ;

Gentile, M .

PRENATAL DIAGNOSIS, 2003, 23 (09) :752-757

[24] DIGEORGE-SYNDROME - PART OF CATCH-22 [J].

WILSON, DI ;

BURN, J ;

SCAMBLER, P ;

GOODSHIP, J .

JOURNAL OF MEDICAL GENETICS, 1993, 30 (10) :852-856

← 1 2 3 →