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40篇 您的检索式：作者名="Faas BH"

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	题名	作者	年代	出处	被引量
1	Detection of fetal RHD-specific sequences in maternal plasma显示文摘	Faas BH Beuling EA Christiaens GC		0，，：	1
2	Rapid methods for targeted prenatal diagnosis of common chromosome aneuploidies 显示文摘	Faas BH Cirigliano V Bui TH	2011	Semin Fetal Neonatal Med2011，16，2：	1
3	Benefits and limitations of whole genome versus targeted approaches for noninvasive prenatal testing for fetal aneuploidies显示文摘	Boon EM Faas BH	2013	Prenat Diagn2013，33，6：	1
4	Identification of clinically significant, submicroscopic chromosome alterations and UPD in foetuses with ultrasound anomaliesusing genome-wide 250 k SNP array analysis显示文摘	Faas BH van der Burgt I Kooper AJ	2010	J Med Genet2010，47，9：	1
5	Rapid methods for targeted prenatal diagnosis of common chromosome aneuploidies显示文摘	Faas BH Cirigliano V Bui TH	2011	Semin Fetal Neonatal Med2011，16，：	1
6	Detection of fetal RHD-specific sequences in maternal plasma显示文摘	Faas BH Beuling EA Christiaens GC	1998	Lancet1998，352，9135：	1
7	Multiplex Ligation- dependent Probe Amplification (MLPA) as a stand - alone test for rapid aneuploidy detection in amniotic fluid cells显示文摘	Kooper AJ Faas BH Kater- Baats E	2008	Prenat Diagn2008，28，11：	1
8	Multiplex ligation-dependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cells显示文摘	Kooper AJ Faas BH Kater-Baats E	2008	Prenat Diagn2008，28，11：	1
9	Rapid methods for targeted prenatal diagnosis of common chromosome aneuploidies显示文摘	Faas BH Cirigliano V Bui TH	2011	Semin Fetal Neonatal Med2011，16，2：	1
10	Detection of fetal RHD-specific sequences in maternal plasma显示文摘	Faas BH Beuling EA Christiaens GC	1998	Lancet1998，352，9135：	1
11	Characterization of the hybrid RHD gene leading to the partial D category Ill c phenotype 显示文摘	Beckers EA Faas BH Ligthart P	1996	Transfusion1996，36，6：	1
12	Multiplex ligationdependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cells显示文摘	Kooper AJ Faas BH Kater-Baats E		0，，：	1
13	Identification of clinically significant,submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis显示文摘	Faas BH van der Burgt I Kooper AJ	2010	J Med Genet2010，47，9：	1
14	Rapid methods for targeted prenatal diagnosis of common chromosome aneuploidies显示文摘	Faas BH Cirigliano V Bui TH	2011	Semin Feta Neonata Med2011，16，2：	1
15	Rapid methods for targetedprenatal diagnosis of common chromosome aneuploidies显示文摘	Faas BH Cirigliano V Bui TH	2011	Semin Fetal Neonatal Med2011，16，2：	1
16	Multiplex ligation-dependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection inamniotic fluid cells显示文摘	Kooper AJ Faas BH Kater-Baats E		0，，11：	1
17	Lower antigen site density and weak D immunogenicity cannot be explained by structural genomie abnormalities or regulatory defects of the RHD gene 显示文摘	Beckers EA Faas BH Ligthart P	1997	Transfusion1997，37，6：	1
18	Benefits and limitations of whole genome versus targeted approaches for noninvasive prenatal testing for fetal aneuploidies显示文摘	Boon EM Faas BH	2013	Prenat Diagn2013，33，6：	1
19	Multiplex ligation-dependent probe amplification(MLPA) as a stand- alone test for rapid aneuploidy detection in amniotic fluid cells 显示文摘	Kooper JA Faas BH Kater-Baats E	2008	Prenat Diagn2008，28，11：	1
20	Rapid methods for targeted prenatal dia- gnosis of common chromosome aneuploidies 显示文摘	Faas BH Cirigliano V Bui TH	2011	Semin Fetal Neonatal Med2011，16，2：	1

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