Baena N - Search Results

1

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. Ann Genet. 2001 Apr-Jun;44(2):83-8. doi: 10.1016/s0003-3995(01)01042-5. Ann Genet. 2001. PMID: 11522246

2

Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21, in a population with a high prevalence of Down syndrome: increased incidence in cases of paternal origin.

Blanco J, Gabau E, Gómez D, Baena N, Guitart M, Egozcue J, Vidal F. Blanco J, et al. Among authors: baena n. Am J Hum Genet. 1998 Oct;63(4):1067-72. doi: 10.1086/302058. Am J Hum Genet. 1998. PMID: 9758616 Free PMC article.

3

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: baena n. Ann Genet. 2000 Jan-Mar;43(1):23-8. doi: 10.1016/s0003-3995(00)00017-4. Ann Genet. 2000. PMID: 10818217

4

Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe.

De Vigan C, Baena N, Cariati E, Clementi M, Stoll C; EUROSCAN Working Group. De Vigan C, et al. Among authors: baena n. Ann Genet. 2001 Oct-Dec;44(4):209-17. doi: 10.1016/s0003-3995(01)01091-7. Ann Genet. 2001. PMID: 11755107

5

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. 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

6

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. 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

7

Contribution of ultrasonographic examination to the prenatal detection of trisomy 21: experience from 19 European registers.

Wellesley D, De Vigan C, Baena N, Cariati E, Stoll C, Boyd PA, Clementi M; Euroscan Group. Wellesley D, et al. Among authors: baena n. Ann Genet. 2004 Oct-Dec;47(4):373-80. doi: 10.1016/j.anngen.2004.09.005. Ann Genet. 2004. PMID: 15581835

8

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: baena n. 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

9

Genetic testing in hereditary breast and ovarian cancer using massive parallel sequencing.

Ruiz A, Llort G, Yagüe C, Baena N, Viñas M, Torra M, Brunet A, Seguí MA, Saigí E, Guitart M. Ruiz A, et al. Among authors: baena n. Biomed Res Int. 2014;2014:542541. doi: 10.1155/2014/542541. Epub 2014 Jun 26. Biomed Res Int. 2014. PMID: 25136594 Free PMC article.

10

A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion.

Viñas-Jornet M, Esteba-Castillo S, Gabau E, Ribas-Vidal N, Baena N, San J, Ruiz A, Coll MD, Novell R, Guitart M. Viñas-Jornet M, et al. Among authors: baena n. Mol Genet Genomic Med. 2014 Nov;2(6):512-21. doi: 10.1002/mgg3.105. Epub 2014 Aug 18. Mol Genet Genomic Med. 2014. PMID: 25614873 Free PMC article.

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