Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1→qter)

被引：7

作者：

Chen, CP ^{[1
]}

Chang, TY

Tzen, CY

Wang, WS

Lee, CC

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, Sch Nursing, Inst Clin Nursing, Taipei 112, Taiwan

[4] China Med Univ, Coll Chinese Med, Taichung, Taiwan

来源：

PRENATAL DIAGNOSIS | 2005年 / 25卷 / 03期

关键词：

D O I：

10.1002/pd.1106

中图分类号：

Q3 [遗传学];

学科分类号：

071007 [遗传学]; 090102 [作物遗传育种];

摘要：

引用

页码：263 / 264

页数：2

共 5 条

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[2]

Fryns JP, 1990, BIRTH DEFECTS ENCY, P359

[3]

De novo der(X)t(X;10) (q26;q21) with features of distal trisomy 10q: Case report of paternal origin identified by late replication with BrdU and the human androgen receptor assay (HAR) [J].

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[5]

Antenatal diagnosis of upper urinary tract dilation by ultrasonography [J].

Langer, B ;

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Montoya, Y ;

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Schlaeder, G .

FETAL DIAGNOSIS AND THERAPY, 1996, 11 (03) :191-198

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