C Cabrol
Overview
Explore the profile of C Cabrol including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
467
Citations
816
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Dubucs C, Chassaing N, Sergi C, Aubert-Mucca M, Attie-Bitach T, Lacombe D, et al.
Clin Oral Investig
. 2020 Jul;
25(3):1353-1362.
PMID: 32643087
Objectives: Agnathia-otocephaly complex is a rare condition characterized by mandibular hypoplasia or agnathia, ear anomalies (melotia/synotia) and microstomia with aglossia. This severe anomaly of the first branchial arch is most...
2.
Brischoux-Boucher E, Trimouille A, Baujat G, Goldenberg A, Schaefer E, Guichard B, et al.
Clin Genet
. 2018 Jun;
94(3-4):373-380.
PMID: 29926465
By describing 10 new patients recruited in centres for Human Genetics, we further delineate the clinical spectrum of a Crouzon-like craniosynostosis disorder, officially termed craniosynostosis and dental anomalies (MIM614188). Singularly,...
3.
Luquet I, Lai J, Barin C, Baranger L, Bilhou-Nabera C, Lippert E, et al.
Leukemia
. 2007 Oct;
22(1):132-7.
PMID: 17928884
A series of 38 patients with acute myeloblastic leukemia (AML) with 49 or more chromosomes and without structural abnormalities was selected within the Groupe Francophone de Cytogénétique Hématologique (GFCH) to...
4.
Romana S, Radford-Weiss I, Ben Abdelali R, Schluth C, Petit A, Dastugue N, et al.
Leukemia
. 2006 Feb;
20(4):696-706.
PMID: 16467868
The NUP98 gene is fused with 19 different partner genes in various human hematopoietic malignancies. In order to gain additional clinico-hematological data and to identify new partners of NUP98, the...
5.
Meyer-Monard S, Parlier V, Passweg J, Muhlematter D, Hess U, Bargetzi M, et al.
Leukemia
. 2006 Jan;
20(2):247-53.
PMID: 16408102
We evaluated the impact of genetic analysis combining cytogenetics and broad molecular screening on leukemia diagnosis according to World Health Organization (WHO) and on genetic risk assignment. A two-step nested...
6.
Lessard M, Struski S, Leymarie V, Flandrin G, Lafage-Pochitaloff M, Mozziconacci M, et al.
Cancer Genet Cytogenet
. 2005 Dec;
163(2):113-22.
PMID: 16337853
Chromosomal abnormalities of erythroleukemia (EL) are often described as complex and unspecific. A retrospective study of 75 EL defined following the WHO classification was performed by the Groupe Francophone de...
7.
Lovey P, Darbellay R, Cabrol C, Roux E, Starobinski M, Helg C, et al.
Eur J Haematol
. 1999 Oct;
63(4):280-1.
PMID: 10530422
No abstract available.
8.
Cools J, Bilhou-Nabera C, Wlodarska I, Cabrol C, Talmant P, Bernard P, et al.
Blood
. 1999 Sep;
94(5):1820-4.
PMID: 10477709
The ETV6 gene (also known as TEL) is the main target of chromosomal translocations affecting chromosome band 12p13. The rearrangements fuse ETV6 to a wide variety of partner genes in...
9.
Cabrol C, Samii K, Scherrer A, Darbellay R, Beris P
Cancer Genet Cytogenet
. 1999 May;
111(2):184-5.
PMID: 10347563
No abstract available.
10.
Laurencet F, Zulian G, Cabrol C, Betticher D
Cancer Genet Cytogenet
. 1997 Nov;
99(1):85-9.
PMID: 9352802
Therapy-related myelodysplastic syndrome (t-MDS) and acute nonlymphocytic leukemia (t-ANLL) are dramatic complications of cancer chemotherapy. Drugs like plant alkaloids or antimetabolites have not been reported to cause either t-MDS or...