Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies

[1] Ekelund C(2008)Impact of a new national screening policy for Down's syndrome in Denmark: population based cohort study BMJ 337 a2547-772

[2] Jørgensen F(2000–2009)Trends in the utilization of invasive prenatal diagnosis in The Netherlands during Prenat Diagn 31 765-101

[3] Petersen O(2011)Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing PLoS One 6 e21791-93

[4] Sundberg K(2011)Targeted massively parallel sequencing of maternal plasma DNA permits efficient and unbiased detection of fetal alleles Clin Chem 57 92-313

[5] Tabor A(2010)Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus Sci Transl Med 2 61-840

[6] Lichtenbelt KD(2011)Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study BMJ 342 c7401-745

[7] Alizadeh BZ(2011)Non-invasive prenatal diagnosis by fetal nucleic acid analysis in maternal plasma: the coming of age Semin Fetal Neonatal Med 16 88-284

[8] Scheffer PG(2011)Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21 Nat Med 17 310-39

[9] Stoutenbeek P(2010)Genetic testing for autism: recent advances and clinical implications Expert Rev Mol Diagn 10 837-541

[10] Schielen PC(2010)Committee PPaG. Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities Genet Med 12 742-594

[1] Ekelund C(2008)Impact of a new national screening policy for Down's syndrome in Denmark: population based cohort study BMJ 337 a2547-772

[2] Jørgensen F(2000–2009)Trends in the utilization of invasive prenatal diagnosis in The Netherlands during Prenat Diagn 31 765-101

[3] Petersen O(2011)Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing PLoS One 6 e21791-93

[4] Sundberg K(2011)Targeted massively parallel sequencing of maternal plasma DNA permits efficient and unbiased detection of fetal alleles Clin Chem 57 92-313

[5] Tabor A(2010)Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus Sci Transl Med 2 61-840

[6] Lichtenbelt KD(2011)Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study BMJ 342 c7401-745

[7] Alizadeh BZ(2011)Non-invasive prenatal diagnosis by fetal nucleic acid analysis in maternal plasma: the coming of age Semin Fetal Neonatal Med 16 88-284

[8] Scheffer PG(2011)Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21 Nat Med 17 310-39

[9] Stoutenbeek P(2010)Genetic testing for autism: recent advances and clinical implications Expert Rev Mol Diagn 10 837-541

[10] Schielen PC(2010)Committee PPaG. Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities Genet Med 12 742-594