717 results on '"Vekemans M"'
Search Results
2. COVID-19: impact of vaccination in myeloma patients
3. Diagnostic Yield of Chromosomal Microarray Analysis in Fetuses With Isolated Increased Nuchal Translucency: A French Multicenter Study
4. Correction: Lenalidomide added to standard intensive treatment for older patients with AML and high-risk MDS
5. Manifestations rares des gammapathies monoclonales : à propos de 2 cas et revue de la littérature
6. Comparative value of post-remission treatment in cytogenetically normal AML subclassified by NPM1 and FLT3-ITD allelic ratio
7. Comparative therapeutic value of post-remission approaches in patients with acute myeloid leukemia aged 40–60 years
8. Three-dimensional reconstruction of the lower limb’s venous system in human fetuses using the computer-assisted anatomical dissection (CAAD) technique
9. Resistance prediction in AML: analysis of 4601 patients from MRC/NCRI, HOVON/SAKK, SWOG and MD Anderson Cancer Center
10. Differential association of calreticulin type 1 and type 2 mutations with myelofibrosis and essential thrombocytemia: relevance for disease evolution
11. Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathy
12. Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasma
13. A general chemotherapy myelotoxicity score to predict febrile neutropenia in hematological malignancies
14. Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): Report of 16 fetal cases
15. Causes of fever in cancer patients (prospective study over 477 episodes)
16. NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique
17. Low mannose-binding lectin concentration is associated with severe infection in patients with hematological cancer who are undergoing chemotherapy
18. La CGH array : un bouleversement de la pratique hospitalière en cytogénétique
19. Febrile neutropenia and Fusobacterium bacteremia: clinical experience with 13 cases
20. OFD1 mutations in males: phenotypic spectrum and ciliary basal body docking impairment
21. Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH
22. Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p
23. Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain
24. Bortezomib (Velcade)-thalidomide-dexamethasone is superior to thalidomide-dexamethasone in patients with multiple myeloma progressing or relapsing after autologous transplantation: 0117
25. LRRFIP1, a new FGFR1 partner gene associated with 8p11 myeloproliferative syndrome
26. Fusion of ZMIZ1 to ABL1 in a B-cell acute lymphoblastic leukaemia with a t(9;10)(q34;q22.3) translocation
27. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies
28. 19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation
29. Rare IgH/14q32 Translocations in Multiple Myeloma: B390
30. Multiple Myeloma in Black Africans: Does It Behave Differently?: A626
31. Osteonecrosis of the Jaw in Multiple Myeloma Patients: Risk Factors of Early ONJ, Decreased Impact After 2005: A120
32. The t(14;20)(q32;q12): A Rare Cytogenetic Change in Multiple Myeloma (MM) Associated with Poor Outcome: A182
33. Diagnostic préimplantatoire
34. Diagnostic génétique préimplantatoire et grossesses spontanées : un passage à l'acte inattendu
35. La CGH microarray : principe et applications en pathologie constitutionnelle
36. L’expérience parisienne du diagnostic génétique pré-implantatoire (DPI) : bilan des premières naissances
37. Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasia
38. Sotos syndrome caused by a paracentric inversion disrupting the NSD1 gene
39. Genotype–phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: cleft palate in SMS is associated with larger deletions
40. Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: A Case Report
41. Scintigraphic imaging of oncogenes with antisense probes: does it make sense?
42. Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders
43. Chimera and other fertilization errors
44. High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts
45. Congenital hyperinsulinism and mosaic abnormalities of the ploidy
46. Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development
47. Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancer
48. Myotonic dystrophy: does it affect ovarian follicular status and responsiveness to controlled ovarian stimulation?
49. Influence of Mannan binding lectin serum levels on the risk of infection during chemotherapy-induced neutropenia in adult haematological cancer patients: O93
50. High-dose chemotherapy and autologous CD34-positive blood stem cell transplantation for multiple myeloma in an HIV carrier
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