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Items: 12

1.

Duplications at 19q13.33 in patients with neurodevelopmental disorders.

Pérez-Palma E, Saarentaus E, Ravoet M, De Ferrari GV, Nürnberg P, Isidor B, Neubauer BA, Lal D.

Neurol Genet. 2018 Jan 26;4(1):e210. doi: 10.1212/NXG.0000000000000210. eCollection 2018 Feb.

2.

Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene.

Lannoy N, Ravoet M, Grisart B, Fretigny M, Vikkula M, Hermans C.

Thromb Res. 2016 Jan;137:224-7. doi: 10.1016/j.thromres.2015.11.015. Epub 2015 Dec 1. No abstract available.

PMID:
26653368
3.

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.

Vanakker O, Vilain C, Janssens K, Van der Aa N, Smits G, Bandelier C, Blaumeiser B, Bulk S, Caberg JH, De Leener A, De Rademaeker M, de Ravel T, Desir J, Destree A, Dheedene A, Gaillez S, Grisart B, Hellin AC, Janssens S, Keymolen K, Menten B, Pichon B, Ravoet M, Revencu N, Rombout S, Staessens C, Van Den Bogaert A, Van Den Bogaert K, Vermeesch JR, Kooy F, Sznajer Y, Devriendt K.

Eur J Med Genet. 2014 Mar;57(4):151-6. doi: 10.1016/j.ejmg.2014.02.002. Epub 2014 Feb 15. Review.

PMID:
24534801
4.

Severe growth retardation, delayed bone age, and facial dysmorphism in two patients with microduplications in 2p16 → p22.

Blassnig-Ezeh A, Bandelier C, Frühmesser A, Revencu N, Krabichler B, Beauloye V, Ravoet M, Fauth C, Zschocke J, Simma B, Kotzot D.

Am J Med Genet A. 2013 Dec;161A(12):3176-81. doi: 10.1002/ajmg.a.36176. Epub 2013 Sep 24.

PMID:
24115558
5.

CD4⁺ follicular helper T cell infiltration predicts breast cancer survival.

Gu-Trantien C, Loi S, Garaud S, Equeter C, Libin M, de Wind A, Ravoet M, Le Buanec H, Sibille C, Manfouo-Foutsop G, Veys I, Haibe-Kains B, Singhal SK, Michiels S, Rothé F, Salgado R, Duvillier H, Ignatiadis M, Desmedt C, Bron D, Larsimont D, Piccart M, Sotiriou C, Willard-Gallo K.

J Clin Invest. 2013 Jul;123(7):2873-92. doi: 10.1172/JCI67428. Epub 2013 Jun 17.

6.

A new case of syndromic craniosynostosis with cryptic 19p13.2-p13.13 deletion.

Lysy PA, Ravoet M, Wustefeld S, Bernard P, Nassogne MC, Wyns E, Sibille C.

Am J Med Genet A. 2009 Nov;149A(11):2564-8. doi: 10.1002/ajmg.a.33056. No abstract available.

PMID:
19842200
7.

Molecular profiling of CD3-CD4+ T cells from patients with the lymphocytic variant of hypereosinophilic syndrome reveals targeting of growth control pathways.

Ravoet M, Sibille C, Gu C, Libin M, Haibe-Kains B, Sotiriou C, Goldman M, Roufosse F, Willard-Gallo K.

Blood. 2009 Oct 1;114(14):2969-83. doi: 10.1182/blood-2008-08-175091. Epub 2009 Jul 16.

8.

Defective CD3gamma gene transcription is associated with NFATc2 overexpression in the lymphocytic variant of hypereosinophilic syndrome.

Willard-Gallo KE, Badran BM, Ravoet M, Zerghe A, Burny A, Martiat P, Goldman M, Roufosse F, Sibille C.

Exp Hematol. 2005 Oct;33(10):1147-59.

PMID:
16219537
9.

6q- is an early and persistent chromosomal aberration in CD3-CD4+ T-cell clones associated with the lymphocytic variant of hypereosinophilic syndrome.

Ravoet M, Sibille C, Roufosse F, Duvillier H, Sotiriou C, Schandené L, Martiat P, Goldman M, Willard-Gallo KE.

Haematologica. 2005 Jun;90(6):753-65.

11.

Analysis of candidate genes included in the mammary cancer susceptibility 1 (Mcs1) region.

Laes JF, Quan X, Ravoet M, Stieber D, Van Vooren P, Van Reeth T, Szpirer J, Szpirer C.

Mamm Genome. 2001 Mar;12(3):199-206.

PMID:
11252168
12.

Localization of new, microdissection- generated, anonymous markers and of the genes Pcsk1, Dhfr, Ndub13, and Ccnb1 to rat chromosome region 2q1.

Quan X, Laes JF, Ravoet M, Van Vooren P, Szpirer J, Szpirer C.

Cytogenet Cell Genet. 2000;88(1-2):119-23.

PMID:
10773684

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