Screen test

被引：6

作者：

Check, E

机构：

[1] Nature's biomedical correspondent,

来源：

NATURE | 2005年 / 438卷 / 7069期

关键词：

D O I：

10.1038/438733a

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

There is a widening gap between geneticists' growing understanding of the roots of disease and their inability to detect those diseases in the womb. A new technique could allow doctors to spot hundreds of potential genetic problems in unborn babies but doctors fear the test could pick up genetic features that are difficult to interpret, causing extra anxiety for parents-to-be.

引用

页码：733 / 734

页数：2

共 6 条

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NATURE, 2005, 437 (7062) :1084-1086

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Pfundt, R ;

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Koolen, DA ;

Vissers, LELM ;

Janssen, IM ;

van Reijmersdal, S ;

Nillesen, WM ;

Huys, EHLPG ;

de Leeuw, N ;

Smeets, D ;

Sistermans, EA ;

Feuth, T ;

van Ravenswaaij-Arts, CMA ;

van Kessel, AG ;

Schoenmakers, EFPM ;

Brunner, HG ;

Veltman, JA .

AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 77 (04) :606-616

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Le Caignec, C ;

Boceno, M ;

Saugier-Veber, P ;

Jacquemont, S ;

Joubert, M ;

David, A ;

Frebourg, T ;

Rival, JM .

JOURNAL OF MEDICAL GENETICS, 2005, 42 (02) :121-128

[5]

RICKMAN L, 2005, J MED GENET

[6] Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features [J].

Shaw-Smith, C ;

Redon, R ;

Rickman, L ;

Rio, M ;

Willatt, L ;

Fiegler, H ;

Firth, H ;

Sanlaville, D ;

Winter, R ;

Colleaux, L ;

Bobrow, M ;

Carter, NP .

JOURNAL OF MEDICAL GENETICS, 2004, 41 (04) :241-248

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