18 results on '"Mugneret, F"'
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2. NUP98is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis
3. Cytogenetic and arrayCGH characterization of a 6q27 deletion in a patient with developmental delay and features of Ehlers–Danlos syndromeHow to cite this article: Mosca AL, Callier P, MasurelPaulet A, ThauvinRobinet C, Marle N, Nouchy M, Huet F, Dipanda D, De Paepe A, Coucke P, Mugneret F, Faivre L. 2010. Cytogenetic and arrayCGH characterization of a 6q27 deletion in a patient with developmental delay and features of Ehlers–Danlos Syndrome. Am J Med Genet Part A 152A:1314–1317.
4. Detection of an interstitial 3q21.1-q21.3 deletion in a child with multiple congenital abnormalities, mental retardation, pancytopenia, and myelodysplasia
5. Polymicrogyria in a child with inv dup del(9p) and 22q11.2 microduplication
6. Array-CGH in a series of 30 patients with mental retardation, dysmorphic features, and congenital malformations detected an interstitial 1p22.2-p31.1 deletion in a patient with features overlapping the Goldenhar syndrome
7. Fortuitous FISH diagnosis of an interstitial microdeletion (5)(q31.1q31.2) in a girl suspected to present a cri-du-chat syndrome
8. Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterization
9. Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome
10. Acute myeloid leukemia with hypergranular cytoplasm: a differential diagnosis of acute promyelocytic leukemia
11. Cytogénétique des syndromes myélodysplasiques
12. Translocation 1;19 in Two Brain Tumors
13. A third tal-1 promoter is specifically used in human T cell leukemias.
14. Epidemiological characteristics of myelodysplastic syndrome in a well-defined French population
15. Vertebral defects as an unusual mode of presentation of 22q11.2 deletion
16. Secondary acute promyelocytic leukemia following irinotecan and oxaliplatin for advanced colon cancer
17. Translocation (21;22)(q22;12) in a Ewing sarcoma: New Case Characterized by Cytogenetic Analysis and Flourescene In Situ Hybridization of a Fresh Tumor
18. Cytogenetic Abnormalities in B-CLL at Binet Stage A: Overview in a Cohort of 484 Untreated Patients and Relations with the ZAP-70 and IgVH Mutation Status.
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