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1.
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.
Am J Hum Genet
; 109(6): 1140-1152, 2022 06 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-35659929
2.
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
Am J Hum Genet
; 105(6): 1091-1101, 2019 12 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-31708118
3.
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.
Am J Hum Genet
; 109(7): 1344, 2022 Jul 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35803237
4.
Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study.
Genet Med
; 20(5): 480-485, 2018 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-29121006
5.
Chromosomal abnormalities and copy number variations in fetal left-sided congenital heart defects.
Prenat Diagn
; 36(2): 177-85, 2016 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-26716421
6.
Economic evaluation of multiplex ligation-dependent probe amplification and karyotyping in prenatal diagnosis: a cost-minimization analysis.
Arch Gynecol Obstet
; 285(1): 67-75, 2012 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-21594605
7.
Isolated Increased Nuchal Translucency in First Trimester Ultrasound Scan: Diagnostic Yield of Prenatal Microarray and Outcome of Pregnancy.
Front Med (Lausanne)
; 8: 737936, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34733861
8.
Multiplex ligation-dependent probe amplification versus karyotyping in prenatal diagnosis: the M.A.K.E. study.
BMC Pregnancy Childbirth
; 8: 18, 2008 May 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-18492228
9.
A prenatal case of partial trisomy 21 (q22.2q22.3), resulting from a paternal insertion translocation ins(16;21) and uncovered by QF-PCR, and characterized by array CGH and FISH.
Clin Case Rep
; 6(7): 1313-1316, 2018 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-29988599
10.
A novel t(6;14)(q25-q27;q32) in acute myelocytic leukemia involves the BCL11B gene.
Cancer Genet Cytogenet
; 149(1): 72-6, 2004 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-15104287
11.
Evaluation of the introduction of the national Down syndrome screening program in the Netherlands: age-related uptake of prenatal screening and invasive diagnostic testing.
Eur J Obstet Gynecol Reprod Biol
; 174: 59-63, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24405726
12.
Monosomal karyotype in acute myeloid leukemia: a better indicator of poor prognosis than a complex karyotype.
J Clin Oncol
; 26(29): 4791-7, 2008 Oct 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-18695255
13.
The heterogeneous distribution of monosomy 3 in uveal melanomas: implications for prognostication based on fine-needle aspiration biopsies.
Arch Pathol Lab Med
; 131(1): 91-6, 2007 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-17227129
14.
Challenging diagnosis in a patient with clear lymphoid immunohistochemical features and myeloid morphology: mixed phenotype acute leukemia with erythrophagocytosis.
Leuk Res
; 35(5): 693-6, 2011 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-21334744
15.
Phenotypic and genomic analysis of an exceptional case of enteropathy associated T-cell lymphoma.
Leuk Res
; 34(8): e183-9, 2010 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-20226524
16.
Alpha-interferon with very-low-dose donor lymphocyte infusion for hematologic or cytogenetic relapse of chronic myeloid leukemia induces rapid and durable complete remissions and is associated with acceptable graft-versus-host disease.
Biol Blood Marrow Transplant
; 10(3): 204-12, 2004 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-14993886
17.
Diabetes insipidus in a child with a monosomy-7 associated myelodysplastic syndrome and neurofibromatosis I.
Med Pediatr Oncol
; 40(4): 257-9, 2003 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-12555259
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