维普期刊资源整合服务平台（V6.5）

83篇 您的检索式：作者名="DEVRIENDT K"

选中清除导出查看参考文献查看引证文献引用追踪共5页首页上一页第1页下一页末页 /5 跳转

	题名	作者	年代	出处	被引量
1	A novel NOG mutation Pro37Arg in a family with tarsal and carpal synostoses显示文摘	Fryns JP Devriendt K	2004	Am J Med Genet A2004，128，：	1
2	Rapid prenatal diagnosis of trisomy21 in 5049 consecutive uncultured amniotie fluid samples by fluorescence in situ hybridisation(FISH)显示文摘	Witters I Devriendt K Legius E	2002	Prenat Diagn2002，22，1：	1
3	Deletion of thy- roid transcription factor-1 gene in an infant with neonatal thyroid dysfunction and respiratory failure 显示文摘	Devriendt K Vanhole C Matthijs G	1998	N Engl J Med1998，338，18：	1
4	Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH) 显示文摘	Witters I Devriendt K Legius E	2002	Prenat Diagn2002，22，1：	1
5	Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridization (FISH) 显示文摘	Witters I Devriendt K Legius E	2002	Prenat Diagn2002，22，：	1
6	Array-based approaches in prenatal diagnosis显示文摘	Brady PD Devriendt K Deprest J	2012	Methods Mol Biol2012，838，：	1
7	Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridization (FISH) 显示文摘	Writters I Devriendt K Legius E	2002	Prenat Diagn2002，22，1：	1
8	Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridization (FISH) 显示文摘	Witters I Devriendt K Legius E	2002	Prenat Diagn2002，22，：	1
9	Mutations in the transcription factor gene SOX18 underlie recessive and dominant fornls of hypotriehosis-lymphedema-telangiectasia 显示文摘	Irrthum A Devriendt K Chitayat D	2003	Am J Hum Genet2003，72，6：	1
10	Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase 显示文摘	Irrthum A Karakkainen MJ Devriendt K	2000	Am J Hum Genet2000，67，：	1
11	Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telan- giectasia显示文摘	Irrthum A Devriendt K Chitayat D	2003	Am J Hum Genet2003，72，6：	1
12	Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridization (FISH)显示文摘	Witters I Devriendt K Legius E	2002	Prenat Diagn2002，22，1：	1
13	1 Congenital hereditarylymph edema caused by a mutation that inactivatesVEGFR3 tyrosine kinase 显示文摘	Irrthum A Karkkainen MJ Devriendt K	2000	l Am J Hum Genet2000，67，：	1
14	Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridization (FISH)显示文摘	WITTERS I DEVRIENDT K LEGIUS E	2002	Prenat Diagn2002，22，1：	1
15	Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridization (FISH)显示文摘	Writters I Devriendt K Legius E	2002	Prenat Diagn2002，22，：	1
16	Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridization(FISH)显示文摘	Writters I Devriendt K Legius E	2002	Prenat Diagn2002，22，1：	1
17	Intellectual abilities in a large sample of children with velo-cardiofacial syndrome:an update显示文摘	Desmedt B Devriendt K Fryns JP	2007	J Intellect Disabil Res2007，51，：	1
18	Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samplesby fluorescence in situ hybridization (FISH) 显示文摘	Witters I Devriendt K Legius E	2002	Prenat Diagrt2002，22，1：	1
19	Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase显示文摘	Irrthum A Karkkainen M J Devriendt K	2000	Am J Hum Genet2000，67，2：	1
20	Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS显示文摘	Swillen A Devriendt K Legius E	1997	J Med Genet1997，34，6：	1

返回顶部每页显示：

共5页首页上一页第1页下一页末页 /5 跳转

互联网出版许可证新出网证(渝)字10号全国400电话 - 免长途话费

用户提示