Rezultati - Lutgarde Govaerts
- Showing 1 - 8 results of 8
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Benefits and Burdens of Using a SNP Array in Pregnancies at Increased Risk for the Common Aneuploidies od Diane Van Opstal, Femke de Vries, Lutgarde Govaerts, Marjan Boter, Debora Lont, Stefanie van Veen, Marieke Joosten, Karin E. M. Diderich, Robert‐Jan Galjaard, Malgorzata I. Srebniak
Izdano 2014Artigo -
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False Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature Review od Diane Van Opstal, Malgorzata I. Srebniak, Joke Polak, Femke de Vries, Lutgarde Govaerts, Marieke Joosten, Attie T. J. I. Go, Maarten F. C. M. Knapen, Cardi van den Berg, Karin E. M. Diderich, Robert-Jan H. Galjaard
Izdano 2016Revisão -
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Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs od Malgorzata I. Srebniak, Karin E. M. Diderich, Marieke Joosten, Lutgarde Govaerts, Jeroen Knijnenburg, Femke At de Vries, Marjan Boter, Debora Lont, Maarten F. C. M. Knapen, M. C. de Wit, Attie T. J. I. Go, Robert‐Jan H. Galjaard, Diane Van Opstal
Izdano 2015Artigo -
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Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities od Malgorzata I. Srebniak, Marjan Boter, Grétel Oudesluijs, Titia E. Cohen‐Overbeek, Lutgarde Govaerts, Karin E. M. Diderich, Renske Oegema, Maarten F. C. M. Knapen, Ingrid M.B.H. van de Laar, Marieke Joosten, Diane Van Opstal, Robert‐Jan H. Galjaard
Izdano 2012Artigo -
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Molecular Cytogenetic Analysis of Eight Inversion Duplications of Human Chromosome 13q That Each Contain a Neocentromere od Peter E. Warburton, Marisa Dolled, Radma Mahmood, Alicia Alonso, Shulan Li, Kenji Naritomi, Takaya Tohma, Toshiro Nagai, Tomonobu Hasegawa, Hirofumi Ohashi, Lutgarde Govaerts, Bert H.J. Eussen, J. O. Van Hemel, Carmen B. Lozzio, Stuart Schwartz, Jennifer J. Dowhanick-Morrissette, Nancy B. Spinner, Horacio Rivera, John A. Crolla, Chih-yu Yu, Dorothy Warburton
Izdano 2000Revisão -
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Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up Study od Catharina J. Heesterbeek, Sietse Aukema, Robert‐Jan H. Galjaard, Elles M. J. Boon, Malgorzata I. Srebniak, Katelijne Bouman, Brigitte H. W. Faas, Lutgarde Govaerts, Mariëtte J.V. Hoffer, Nicolette S. den Hollander, Klaske D. Lichtenbelt, Merel C. van Maarle, Lisanne van Prooyen Schuurman, Maartje C. van Rij, G. Heleen Schuring‐Blom, Servi J.C. Stevens, Gita Tan-Sindhunata, Masoud Zamani Esteki, Christine de Die‐Smulders, Vivianne C. G. Tjan‐Heijnen, Lidewij Henneman, Erik A. Sistermans, Merryn Macville
Izdano 2022Artigo -
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Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study od Diane Van Opstal, Merel C. van Maarle, Klaske D. Lichtenbelt, Marjan M. Weiss, Heleen Schuring‐Blom, Shama L. Bhola, Mariëtte J.V. Hoffer, Karin Huijsdens–van Amsterdam, Merryn Macville, Angelique J. A. Kooper, Brigitte H. W. Faas, Lutgarde Govaerts, Gita Tan-Sindhunata, Nicolette S. den Hollander, Ilse Feenstra, Robert‐Jan H. Galjaard, Dick Oepkes, Stijn A.I. Ghesquiere, Rutger W. W. Brouwer, Lean Beulen, Sander Bollen, Martin Elferink, Roy Straver, Lidewij Henneman, Godelieve C.M.L. Page‐Christiaens, Erik A. Sistermans
Izdano 2017Artigo
Iskalna orodja:
Sorodne teme
Biology
Chromosome
Gene
Genetics
Medicine
Aneuploidy
Fetus
Karyotype
Pregnancy
Genotype
Obstetrics
Pathology
Prenatal diagnosis
SNP
SNP array
Single-nucleotide polymorphism
Abnormality
Genetic testing
Psychiatry
Trisomy
Genetic counseling
Genome
Internal medicine
Placenta
Amniocentesis
Autosome
Bioinformatics
Cancer
Cell-free fetal DNA
Centromere