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68篇 您的检索式：作者名="Veyver"

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	题名	作者	年代	出处	被引量
1	The use of Kleihauer-Betke stain in pregnant patients with abdominal trauma显示文摘	Van den Veyver I Saade G Lockett L	1993	Am J Obstet Gynecol1993，168，：	1
2	Multiplex ligation - depend- ent probe amplification (MLPA) and prenatal diagnosis 显示文摘	Willis A S van den Veyver I Eng C M	2012	Prenat Diagn2012，32，4：	1
3	Clinical use of array competitive genomic hybridization (aCGH) for prenatal diagnosis in 300 cases显示文摘	Van den Veyver IB Patel A Shaw CA	2009	Prenat Diagn2009，29，：	1
4	Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG- binding protein 2 显示文摘	Amir RE Van Den Veyver IB Wan M	1999	Nat Genet1999，23，2：	1
5	Ophthalmologic findings in Aicardi syndrome显示文摘	Gary Fruhman Tanya N. Eble Nikki Gambhir V. Reid Sutton Ignatia B. Van den Veyver Richard A. Lewis	2012	Journal of AAPOS2012，，3：	1
6	Neuroimaging aspects of Aicardi syndrome显示文摘	BobbiHopkins V. ReidSutton Richard AlanLewis IgnatiaVan den Veyver GaryClark	2008	Am J Med Genet2008，，22：	1
7	Facial and physical features of Aicardi syndrome: Infants to teenagers显示文摘	V. ReidSutton Bobbi J.Hopkins Tanya N.Eble NikkiGambhir Richard A.Lewis Ignatia B.Van den Veyver	2005	Am J Med Genet2005，，3：	1
8	A mutant form of MeCP2 protein associated with human rett syndrome cannot be displaced from methylated DNA by Notch in Xenopus embryos显示文摘	Stancheva I Collins AL van den Veyver IB		0，，02：	1
9	Rett syndrome is caused by mutations on X-linked MECP2, encoding methyl-CpGbinding protein 2 显示文摘	Amir RE Van Den Veyver IB Wan M	1999	Nat Genet1999，23，：	1
10	Genetic basis of Rett syndrome显示文摘	Ignatia B Van Den Veyver Aoghbi HY	2002	Mental Retard Dev Dis2002，8，：	1
11	Rett syndrome is caused by mutations on X-linked MECP2, encoding methyl-CpG-binding protein 2显示文摘	Amir RE Van den Veyver IB Wan M	1999	Nat Genet1999，23，2：	1
12	Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2显示文摘	Amir RE Van den Veyver IB Wan M Tran CQ Francke U Zoghbi HY	1999	Nat Genet1999，23，2：	1
13	Rett syndrome is caused by mutations on X-linked MECP2,encoding methyl-CpG-binding protein 2显示文摘	Amir RE Van den Veyver IB Wan M	1999	Nat Genet1999，23，：	1
14	Multiplex ligationdependent probe amplification (MLPA) and prenatal diagnosis显示文摘	Willis AS van den Veyver I Eng CM		0，，：	1
15	Genetic basis of Rett syndrome显示文摘	Van Den Veyver IB Zoghbi HY	2002	Meutal Retard Dev Dis2002，8，2：	1
16	Treatment of polyhydramnios with indomethacin显示文摘	Kramer WB Van den Veyver IB Kirshon B	1994	Clin Perinatol1994，21，3：	1
17	Clinical use of array compatative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases显示文摘	Van den Veyver I B Pate1 A Shaw C A	2009	Prenat Diagn2009，29，1：	1
18	Rett syndrome is caused by mutations in X-linked MECP2,encoding methyl-CpGbinding protein 2显示文摘	Amir RE Van den Veyver IB Wan M	1999	Nat Genet1999，23，：	1
19	Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG- binding orotein 2 显示文摘	Amir RE Van den Veyver IB Wan M	1999	Nat Genet1999，23，2：	1
20	Multiplex ligation-dependent probe amplification (MLPA) and prenatal diagnosis显示文摘	Willis AS van den Veyver I Eng CM		0，，04：	1

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