Caballin MR - Search Results

1

Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome.

Belloso JM, Bache I, Guitart M, Caballin MR, Halgren C, Kirchhoff M, Ropers HH, Tommerup N, Tümer Z. Belloso JM, et al. Among authors: caballin mr. Eur J Hum Genet. 2007 Jun;15(6):711-3. doi: 10.1038/sj.ejhg.5201824. Epub 2007 Mar 28. Eur J Hum Genet. 2007. PMID: 17392702

2

Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.

Brunet A, Gabau E, Perich RM, Valdesoiro L, Brun C, Caballín MR, Guitart M. Brunet A, et al. Among authors: caballin mr. Am J Med Genet A. 2006 Nov 15;140(22):2426-32. doi: 10.1002/ajmg.a.31499. Am J Med Genet A. 2006. PMID: 17041934

3

Characterization of six marker chromosomes by comparative genomic hybridization.

Belloso JM, Caballín MR, Gabau E, Baena N, Vidal R, Villatoro S, Guitart M. Belloso JM, et al. Among authors: caballin mr. Am J Med Genet A. 2005 Jul 15;136(2):169-74. doi: 10.1002/ajmg.a.30788. Am J Med Genet A. 2005. PMID: 15948187

4

Genetic abnormalities associated with the t(12;21) and their impact in the outcome of 56 patients with B-precursor acute lymphoblastic leukemia.

Alvarez Y, Coll MD, Ortega JJ, Bastida P, Dastugue N, Robert A, Cervera J, Verdeguer A, Tasso M, Aventín A, Guitart M, Caballín MR. Alvarez Y, et al. Among authors: caballin mr. Cancer Genet Cytogenet. 2005 Oct 1;162(1):21-9. doi: 10.1016/j.cancergencyto.2005.02.019. Cancer Genet Cytogenet. 2005. PMID: 16157196

5

Origin of trisomy 21 in Down syndrome cases from a Spanish population registry.

Gómez D, Solsona E, Guitart M, Baena N, Gabau E, Egozcue J, Caballín MR. Gómez D, et al. Among authors: caballin mr. Ann Genet. 2000 Jan-Mar;43(1):23-8. doi: 10.1016/s0003-3995(00)00017-4. Ann Genet. 2000. PMID: 10818217

6

Presenting features of 201 children with acute lymphoblastic leukemia: comparison according to presence or absence of ETV6/RUNX1 rearrangement.

Alvarez Y, Caballín MR, Gaitán S, Pérez A, Bastida P, Ortega JJ, Cervera J, Verdeguer A, Tasso M, Aventín A, Badell I, Guitart M, Melo M, Granada I, Javier G, Dastugue N, Robert A, Coll MD. Alvarez Y, et al. Among authors: caballin mr. Cancer Genet Cytogenet. 2007 Sep;177(2):161-3. doi: 10.1016/j.cancergencyto.2007.05.012. Cancer Genet Cytogenet. 2007. PMID: 17854676 No abstract available.

7

Turner syndrome: evaluation of prenatal diagnosis in 19 European registries.

Baena N, De Vigan C, Cariati E, Clementi M, Stoll C, Caballín MR, Guitart M. Baena N, et al. Among authors: caballin mr. Am J Med Genet A. 2004 Aug 15;129A(1):16-20. doi: 10.1002/ajmg.a.30092. Am J Med Genet A. 2004. PMID: 15266609

8

Prenatal detection of rare chromosomal autosomal abnormalities in Europe.

Baena N, De Vigan C, Cariati E, Clementi M, Stoll C, Caballin MR, Guitart M; EUROSCAN Working Group. Baena N, et al. Among authors: caballin mr. Am J Med Genet A. 2003 May 1;118A(4):319-27. doi: 10.1002/ajmg.a.10104. Am J Med Genet A. 2003. PMID: 12687662

9

A new balanced (1;22)(p22;q13) translocation in a sterile male.

Miró R, Caballín MR, Pomerol JM, Egozcue J. Miró R, et al. Among authors: caballin mr. Hum Genet. 1985;71(4):372. doi: 10.1007/BF00388469. Hum Genet. 1985. PMID: 4077055 No abstract available.

10

Fetal and placenta chromosome constitution in 237 pregnancy losses.

Baena N, Guitart M, Ferreres JC, Gabau E, Corona M, Mellado F, Egozcue J, Caballín MR. Baena N, et al. Among authors: caballin mr. Ann Genet. 2001 Apr-Jun;44(2):83-8. doi: 10.1016/s0003-3995(01)01042-5. Ann Genet. 2001. PMID: 11522246

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