Amy Breman, Amber N Pursley, Patricia Hixson, Weimin Bi, Patricia Ward, Carlos A Bacino, Chad Shaw, James R Lupski, Arthur Beaudet, Ankita Patel, Sau W Cheung, Ignatia Van den Veyver. Prenat Diagn 2012
Times Cited: 74
Times Cited: 74
Times Cited
Times Co-cited
Similarity
Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
70
Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies.
Lisa G Shaffer, Mindy P Dabell, Allan J Fisher, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Jill A Rosenfeld. Prenat Diagn 2012
Lisa G Shaffer, Mindy P Dabell, Allan J Fisher, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Jill A Rosenfeld. Prenat Diagn 2012
45
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
39
Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.
C-N Lee, S-Y Lin, C-H Lin, J-C Shih, T-H Lin, Y-N Su. BJOG 2012
C-N Lee, S-Y Lin, C-H Lin, J-C Shih, T-H Lin, Y-N Su. BJOG 2012
37
Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases.
Francesco Fiorentino, Fiorina Caiazzo, Stefania Napolitano, Letizia Spizzichino, Sara Bono, Mariateresa Sessa, Andrea Nuccitelli, Anil Biricik, Anthony Gordon, Giuseppe Rizzo,[...]. Prenat Diagn 2011
Francesco Fiorentino, Fiorina Caiazzo, Stefania Napolitano, Letizia Spizzichino, Sara Bono, Mariateresa Sessa, Andrea Nuccitelli, Anil Biricik, Anthony Gordon, Giuseppe Rizzo,[...]. Prenat Diagn 2011
31
Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
29
Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.
S C Hillman, S Pretlove, A Coomarasamy, D J McMullan, E V Davison, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2011
S C Hillman, S Pretlove, A Coomarasamy, D J McMullan, E V Davison, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2011
28
Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis.
Lluís Armengol, Julián Nevado, Clara Serra-Juhé, Alberto Plaja, Carmen Mediano, Fe Amalia García-Santiago, Manel García-Aragonés, Olaya Villa, Elena Mansilla, Cristina Preciado,[...]. Hum Genet 2012
Lluís Armengol, Julián Nevado, Clara Serra-Juhé, Alberto Plaja, Carmen Mediano, Fe Amalia García-Santiago, Manel García-Aragonés, Olaya Villa, Elena Mansilla, Cristina Preciado,[...]. Hum Genet 2012
32
Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
Ignatia B Van den Veyver, Ankita Patel, Chad A Shaw, Amber N Pursley, Sung-Hae L Kang, Marcia J Simovich, Patricia A Ward, Sandra Darilek, Anthony Johnson, Sarah E Neill,[...]. Prenat Diagn 2009
Ignatia B Van den Veyver, Ankita Patel, Chad A Shaw, Amber N Pursley, Sung-Hae L Kang, Marcia J Simovich, Patricia A Ward, Sandra Darilek, Anthony Johnson, Sarah E Neill,[...]. Prenat Diagn 2009
24
Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
23
Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.
Francesco Fiorentino, Stefania Napoletano, Fiorina Caiazzo, Mariateresa Sessa, Sara Bono, Letizia Spizzichino, Anthony Gordon, Andrea Nuccitelli, Giuseppe Rizzo, Marina Baldi. Eur J Hum Genet 2013
Francesco Fiorentino, Stefania Napoletano, Fiorina Caiazzo, Mariateresa Sessa, Sara Bono, Letizia Spizzichino, Anthony Gordon, Andrea Nuccitelli, Giuseppe Rizzo, Marina Baldi. Eur J Hum Genet 2013
26
Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis.
B H W Faas, I van der Burgt, A J A Kooper, R Pfundt, J Y Hehir-Kwa, A P T Smits, N de Leeuw. J Med Genet 2010
B H W Faas, I van der Burgt, A J A Kooper, R Pfundt, J Y Hehir-Kwa, A P T Smits, N de Leeuw. J Med Genet 2010
20
High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings.
M Tyreman, K M Abbott, L R Willatt, R Nash, C Lees, J Whittaker, I Simonic. J Med Genet 2009
M Tyreman, K M Abbott, L R Willatt, R Nash, C Lees, J Whittaker, I Simonic. J Med Genet 2009
20
Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray.
Justine Coppinger, Sarah Alliman, Allen N Lamb, Beth S Torchia, Bassem A Bejjani, Lisa G Shaffer. Prenat Diagn 2009
Justine Coppinger, Sarah Alliman, Allen N Lamb, Beth S Torchia, Bassem A Bejjani, Lisa G Shaffer. Prenat Diagn 2009
18
Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases.
Sang-Jin Park, Eun Hye Jung, Ran-Suk Ryu, Hyun Woong Kang, Jung-Min Ko, Hyon J Kim, Chong Kun Cheon, Sang-Hyun Hwang, Ho-Young Kang. Mol Cytogenet 2011
Sang-Jin Park, Eun Hye Jung, Ran-Suk Ryu, Hyun Woong Kang, Jung-Min Ko, Hyon J Kim, Chong Kun Cheon, Sang-Hyun Hwang, Ho-Young Kang. Mol Cytogenet 2011
23
American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
18
Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.
Trilochan Sahoo, Sau Wai Cheung, Patricia Ward, Sandra Darilek, Ankita Patel, Daniela del Gaudio, Sung Hae L Kang, Seema R Lalani, Jiangzhen Li, Sallie McAdoo,[...]. Genet Med 2006
Trilochan Sahoo, Sau Wai Cheung, Patricia Ward, Sandra Darilek, Ankita Patel, Daniela del Gaudio, Sung Hae L Kang, Seema R Lalani, Jiangzhen Li, Sallie McAdoo,[...]. Genet Med 2006
17
Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
17
Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype.
Linda Kleeman, Diana W Bianchi, Lisa G Shaffer, Emily Rorem, Janet Cowan, Sabrina D Craigo, Hocine Tighiouart, Louise E Wilkins-Haug. Prenat Diagn 2009
Linda Kleeman, Diana W Bianchi, Lisa G Shaffer, Emily Rorem, Janet Cowan, Sabrina D Craigo, Hocine Tighiouart, Louise E Wilkins-Haug. Prenat Diagn 2009
16
Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.
Idit Maya, Bella Davidov, Liron Gershovitz, Yael Zalzstein, Ellen Taub, Justine Coppinger, Lisa G Shaffer, Mordechai Shohat. Prenat Diagn 2010
Idit Maya, Bella Davidov, Liron Gershovitz, Yael Zalzstein, Ellen Taub, Justine Coppinger, Lisa G Shaffer, Mordechai Shohat. Prenat Diagn 2010
19
The introduction of arrays in prenatal diagnosis: a special challenge.
Annalisa Vetro, Katelijne Bouman, Ros Hastings, Dominic J McMullan, Joris R Vermeesch, Konstantin Miller, Birgit Sikkema-Raddatz, David H Ledbetter, Orsetta Zuffardi, Conny M A van Ravenswaaij-Arts. Hum Mutat 2012
Annalisa Vetro, Katelijne Bouman, Ros Hastings, Dominic J McMullan, Joris R Vermeesch, Konstantin Miller, Birgit Sikkema-Raddatz, David H Ledbetter, Orsetta Zuffardi, Conny M A van Ravenswaaij-Arts. Hum Mutat 2012
23
Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities.
Melanie Manning, Louanne Hudgins. Genet Med 2010
Melanie Manning, Louanne Hudgins. Genet Med 2010
16
Committee Opinion No. 581: the use of chromosomal microarray analysis in prenatal diagnosis.
. Obstet Gynecol 2013
. Obstet Gynecol 2013
16
Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial.
Ronald J Wapner, Deborah A Driscoll, Joe Leigh Simpson. Prenat Diagn 2012
Ronald J Wapner, Deborah A Driscoll, Joe Leigh Simpson. Prenat Diagn 2012
25
Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations.
C Le Caignec, M Boceno, P Saugier-Veber, S Jacquemont, M Joubert, A David, T Frebourg, J M Rival. J Med Genet 2005
C Le Caignec, M Boceno, P Saugier-Veber, S Jacquemont, M Joubert, A David, T Frebourg, J M Rival. J Med Genet 2005
14
Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
14
Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
G D'Amours, Z Kibar, G Mathonnet, R Fetni, F Tihy, V Désilets, S Nizard, J L Michaud, E Lemyre. Clin Genet 2012
G D'Amours, Z Kibar, G Mathonnet, R Fetni, F Tihy, V Désilets, S Nizard, J L Michaud, E Lemyre. Clin Genet 2012
17
ACOG Committee Opinion No. 446: array comparative genomic hybridization in prenatal diagnosis.
. Obstet Gynecol 2009
. Obstet Gynecol 2009
13
Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens.
Lisa G Shaffer, Justine Coppinger, Sarah Alliman, Beth A Torchia, Aaron Theisen, Blake C Ballif, Bassem A Bejjani. Prenat Diagn 2008
Lisa G Shaffer, Justine Coppinger, Sarah Alliman, Beth A Torchia, Aaron Theisen, Blake C Ballif, Bassem A Bejjani. Prenat Diagn 2008
13
Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound.
Lisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Allan J Fisher. Prenat Diagn 2012
Lisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Allan J Fisher. Prenat Diagn 2012
13
Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.
Malgorzata I Srebniak, Marjan Boter, Gretel O Oudesluijs, Titia Cohen-Overbeek, Lutgarde Cp Govaerts, Karin Em Diderich, Renske Oegema, Maarten Fcm Knapen, Ingrid Mbh van de Laar, Marieke Joosten,[...]. Mol Cytogenet 2012
Malgorzata I Srebniak, Marjan Boter, Gretel O Oudesluijs, Titia Cohen-Overbeek, Lutgarde Cp Govaerts, Karin Em Diderich, Renske Oegema, Maarten Fcm Knapen, Ingrid Mbh van de Laar, Marieke Joosten,[...]. Mol Cytogenet 2012
19
Karyotype versus microarray testing for genetic abnormalities after stillbirth.
Uma M Reddy, Grier P Page, George R Saade, Robert M Silver, Vanessa R Thorsten, Corette B Parker, Halit Pinar, Marian Willinger, Barbara J Stoll, Josefine Heim-Hall,[...]. N Engl J Med 2012
Uma M Reddy, Grier P Page, George R Saade, Robert M Silver, Vanessa R Thorsten, Corette B Parker, Halit Pinar, Marian Willinger, Barbara J Stoll, Josefine Heim-Hall,[...]. N Engl J Med 2012
13
A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors.
Paul Daniel Brady, Barbara Delle Chiaie, Gabrielle Christenhusz, Kris Dierickx, Kris Van Den Bogaert, Bjorn Menten, Sandra Janssens, Paul Defoort, Ellen Roets, Elke Sleurs,[...]. Genet Med 2014
Paul Daniel Brady, Barbara Delle Chiaie, Gabrielle Christenhusz, Kris Dierickx, Kris Van Den Bogaert, Bjorn Menten, Sandra Janssens, Paul Defoort, Ellen Roets, Elke Sleurs,[...]. Genet Med 2014
22
A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
12
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011.
A Novelli, F R Grati, L Ballarati, L Bernardini, D Bizzoco, L Camurri, R Casalone, L Cardarelli, P Cavalli, R Ciccone,[...]. Ultrasound Obstet Gynecol 2012
A Novelli, F R Grati, L Ballarati, L Bernardini, D Bizzoco, L Camurri, R Casalone, L Cardarelli, P Cavalli, R Ciccone,[...]. Ultrasound Obstet Gynecol 2012
20
Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases.
F Scott, K Murphy, L Carey, W Greville, N Mansfield, P Barahona, R Robertson, A McLennan. Ultrasound Obstet Gynecol 2013
F Scott, K Murphy, L Carey, W Greville, N Mansfield, P Barahona, R Robertson, A McLennan. Ultrasound Obstet Gynecol 2013
20
The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature.
Jonathan L A Callaway, Lisa G Shaffer, Lyn S Chitty, Jill A Rosenfeld, John A Crolla. Prenat Diagn 2013
Jonathan L A Callaway, Lisa G Shaffer, Lyn S Chitty, Jill A Rosenfeld, John A Crolla. Prenat Diagn 2013
12
Referral patterns for microarray testing in prenatal diagnosis.
Lisa G Shaffer, Mindy Preston Dabell, Jill A Rosenfeld, Nicholas J Neill, Blake C Ballif, Justine Coppinger, Noa Rinzler Diwan, Karen Chong, Mordechai Shohat, David Chitayat. Prenat Diagn 2012
Lisa G Shaffer, Mindy Preston Dabell, Jill A Rosenfeld, Nicholas J Neill, Blake C Ballif, Justine Coppinger, Noa Rinzler Diwan, Karen Chong, Mordechai Shohat, David Chitayat. Prenat Diagn 2012
29
A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformations.
M Valduga, C Philippe, P Bach Segura, O Thiebaugeorges, A Miton, M Beri, C Bonnet, C Nemos, B Foliguet, P Jonveaux. Prenat Diagn 2010
M Valduga, C Philippe, P Bach Segura, O Thiebaugeorges, A Miton, M Beri, C Bonnet, C Nemos, B Foliguet, P Jonveaux. Prenat Diagn 2010
14
Use of array genomic hybridization technology in prenatal diagnosis in Canada.
Alessandra Duncan, Sylvie Langlois. J Obstet Gynaecol Can 2011
Alessandra Duncan, Sylvie Langlois. J Obstet Gynaecol Can 2011
38
Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature.
M C de Wit, M I Srebniak, L C P Govaerts, D Van Opstal, R J H Galjaard, A T J I Go. Ultrasound Obstet Gynecol 2014
M C de Wit, M I Srebniak, L C P Govaerts, D Van Opstal, R J H Galjaard, A T J I Go. Ultrasound Obstet Gynecol 2014
10
Benefits and burdens of using a SNP array in pregnancies at increased risk for the common aneuploidies.
Diane Van Opstal, Femke de Vries, Lutgarde Govaerts, Marjan Boter, Debora Lont, Stefanie van Veen, Marieke Joosten, Karin Diderich, Robert-Jan Galjaard, Malgorzata I Srebniak. Hum Mutat 2015
Diane Van Opstal, Femke de Vries, Lutgarde Govaerts, Marjan Boter, Debora Lont, Stefanie van Veen, Marieke Joosten, Karin Diderich, Robert-Jan Galjaard, Malgorzata I Srebniak. Hum Mutat 2015
19
Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.
Malgorzata I Srebniak, Karin Em Diderich, Marieke Joosten, Lutgarde Cp Govaerts, Jeroen Knijnenburg, Femke At de Vries, Marjan Boter, Debora Lont, Maarten Fcm Knapen, Merel C de Wit,[...]. Eur J Hum Genet 2016
Malgorzata I Srebniak, Karin Em Diderich, Marieke Joosten, Lutgarde Cp Govaerts, Jeroen Knijnenburg, Femke At de Vries, Marjan Boter, Debora Lont, Maarten Fcm Knapen, Merel C de Wit,[...]. Eur J Hum Genet 2016
21
Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defects.
Maximilian Schmid, Susanne Stary, Wibke Blaicher, Michaela Gollinger, Peter Husslein, Berthold Streubel. Prenat Diagn 2012
Maximilian Schmid, Susanne Stary, Wibke Blaicher, Michaela Gollinger, Peter Husslein, Berthold Streubel. Prenat Diagn 2012
26
25
Array comparative genomic hybridization in prenatal diagnosis: another experience.
F Vialard, D Molina Gomes, B Leroy, E Quarello, A Escalona, C Le Sciellour, V Serazin, J Roume, Y Ville, P de Mazancourt,[...]. Fetal Diagn Ther 2009
F Vialard, D Molina Gomes, B Leroy, E Quarello, A Escalona, C Le Sciellour, V Serazin, J Roume, Y Ville, P de Mazancourt,[...]. Fetal Diagn Ther 2009
12
Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations.
Paola Evangelidou, Carolina Sismani, Marios Ioannides, Christodoulos Christodoulou, George Koumbaris, Ioannis Kallikas, Ioannis Georgiou, Voula Velissariou, Philippos C Patsalis. Mol Cytogenet 2010
Paola Evangelidou, Carolina Sismani, Marios Ioannides, Christodoulos Christodoulou, George Koumbaris, Ioannis Kallikas, Ioannis Georgiou, Voula Velissariou, Philippos C Patsalis. Mol Cytogenet 2010
22
Prenatal detection of unbalanced chromosomal rearrangements by array CGH.
L Rickman, H Fiegler, C Shaw-Smith, R Nash, V Cirigliano, G Voglino, B L Ng, C Scott, J Whittaker, M Adinolfi,[...]. J Med Genet 2006
L Rickman, H Fiegler, C Shaw-Smith, R Nash, V Cirigliano, G Voglino, B L Ng, C Scott, J Whittaker, M Adinolfi,[...]. J Med Genet 2006
9
Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow.
Malgorzata Srebniak, Marjan Boter, Grétel Oudesluijs, Marieke Joosten, Lutgarde Govaerts, Diane Van Opstal, Robert-Jan H Galjaard. Eur J Hum Genet 2011
Malgorzata Srebniak, Marjan Boter, Grétel Oudesluijs, Marieke Joosten, Lutgarde Govaerts, Diane Van Opstal, Robert-Jan H Galjaard. Eur J Hum Genet 2011
9
Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype.
T Y Leung, I Vogel, T K Lau, W Chong, J A Hyett, O B Petersen, K W Choy. Ultrasound Obstet Gynecol 2011
T Y Leung, I Vogel, T K Lau, W Chong, J A Hyett, O B Petersen, K W Choy. Ultrasound Obstet Gynecol 2011
9
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.