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1.
Involvement of the JAK-STAT pathway in the molecular landscape of tyrosine kinase fusion-negative hypereosinophilic syndromes: A nationwide CEREO study.
Am J Hematol
; 99(6): 1108-1118, 2024 Jun.
Article
in English
| MEDLINE | ID: mdl-38563187
2.
Myeloid malignancies with translocation t(4;12)(q11-13;p13): molecular landscape, clonal hierarchy and clinical outcomes.
J Cell Mol Med
; 25(20): 9557-9566, 2021 10.
Article
in English
| MEDLINE | ID: mdl-34492730
3.
The first familial case of inherited 2q37.3 interstitial deletion with isolated skeletal abnormalities including brachydactyly type E and short stature.
Am J Med Genet A
; 167A(1): 185-9, 2015 Jan.
Article
in English
| MEDLINE | ID: mdl-25402011
4.
Cytogenetics in the management of myeloproliferative neoplasms, mastocytosis and myelodysplastic/myeloproliferative neoplasms: Guidelines from the Group Francophone de Cytogénétique Hématologique (GFCH).
Curr Res Transl Med
; 71(4): 103424, 2023.
Article
in English
| MEDLINE | ID: mdl-38011761
5.
Cytogenetics in the management of acute myeloid leukemia and histiocytic/dendritic cell neoplasms: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH).
Curr Res Transl Med
; 71(4): 103421, 2023.
Article
in English
| MEDLINE | ID: mdl-38016419
6.
French guidelines for the etiological workup of eosinophilia and the management of hypereosinophilic syndromes.
Orphanet J Rare Dis
; 18(1): 100, 2023 04 30.
Article
in English
| MEDLINE | ID: mdl-37122022
7.
Array CGH analysis in high-risk pregnancies: comparing DNA from cultured cells and cell-free fetal DNA.
Prenat Diagn
; 32(4): 383-8, 2012 Apr.
Article
in English
| MEDLINE | ID: mdl-22025315
8.
USAID Associated with Myeloid Neoplasm and VEXAS Syndrome: Two Differential Diagnoses of Suspected Adult Onset Still's Disease in Elderly Patients.
J Clin Med
; 10(23)2021 Nov 27.
Article
in English
| MEDLINE | ID: mdl-34884286
9.
High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B.
Bone
; 123: 145-152, 2019 06.
Article
in English
| MEDLINE | ID: mdl-30905746
10.
21q21 deletion involving NCAM2: report of 3 cases with neurodevelopmental disorders.
Eur J Med Genet
; 58(1): 44-6, 2015 Jan.
Article
in English
| MEDLINE | ID: mdl-25464110
11.
Growth hormone deficiency and pituitary malformation in a recurrent Cat-Eye syndrome: a family report.
Ann Endocrinol (Paris)
; 76(5): 629-34, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-26518262
12.
15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients.
Eur J Med Genet
; 58(3): 140-7, 2015 Mar.
Article
in English
| MEDLINE | ID: mdl-25596525
13.
Successful Imatinib therapy as a bridge to transplant in an atypical myeloproliferative neoplasm.
Curr Res Transl Med
; 67(4): 149-151, 2019 11.
Article
in English
| MEDLINE | ID: mdl-31153956
14.
12q21 Microdeletion in a fetus with Meckel syndrome involving CEP290/MKS4.
Eur J Med Genet
; 56(10): 580-3, 2013 Oct.
Article
in English
| MEDLINE | ID: mdl-23954617
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