Wide scope prenatal diagnosis at Kuopio University Hospital 1997-1998: integration of gene tests and fetal karyotyping-Reference-Cited by-同舟云学术

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Wide scope prenatal diagnosis at Kuopio University Hospital 1997-1998: integration of gene tests and fetal karyotyping

Published:2001-05 Issue:5 Volume:108 Page:505-509
ISSN:1470-0328
Container-title:BJOG: An International Journal of Obstetrics and Gynaecology
language:en
Short-container-title:BJOG: An Internal Journal of Obs Gyn

Author:

Kallinen Juuso,Marin Katja,Heinonen Seppo,Mannermaa Arto,Palotie Aarno,Ryynanen Markku

Publisher

Wiley

Subject

Obstetrics and Gynaecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-0528.2001.00118.x/fullpdf

Reference23 articles.

1. A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE

2. LATE INFANTILE PROGRESSIVE ENCEPHALOPATHY WITH DISTURBED POLYUNSATURATED FAT METABOLISM

3. Molecular genetics of the Finnishdisease heritage

4. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Maternal attitudes to newborn screening for fragile X syndrome;American Journal of Medical Genetics Part A;2013-01-09

2. FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States;Genome Medicine;2012

3. Carrier screening in preconception consultation in primary care;Journal of Community Genetics;2011-12-20

4. A systematic review of population screening for fragile X syndrome;Genetics in Medicine;2010-07

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