Melo JB - Search Results

1

Genetic and epigenetic characterization of the tumors in a patient with a tongue primary tumor, a recurrence and a pharyngoesophageal second primary tumor.

Ribeiro IP, Marques F, Barroso L, Miguéis J, Caramelo F, Santos A, Julião MJ, Melo JB, Carreira IM. Ribeiro IP, et al. Among authors: melo jb. Mol Cytogenet. 2017 Apr 11;10:13. doi: 10.1186/s13039-017-0310-z. eCollection 2017. Mol Cytogenet. 2017. PMID: 28413448 Free PMC article.

2

Three unusual but cytogenetically similar cases with up to five different cell lines involving structural and numerical abnormalities of chromosome 18.

Carreira IM, Mascarenhas A, Matoso E, Couceiro AB, Ramos L, Dufke A, Mazauric M, Stressig R, Kosyakova N, Melo JB, Liehr T. Carreira IM, et al. Among authors: melo jb. J Histochem Cytochem. 2007 Nov;55(11):1123-8. doi: 10.1369/jhc.7A7244.2007. Epub 2007 Jun 26. J Histochem Cytochem. 2007. PMID: 17595336 Free PMC article.

3

First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q.

Mascarenhas A, Matoso E, Saraiva J, Tönnies H, Gerlach A, Julião MJ, Melo JB, Carreira IM. Mascarenhas A, et al. Among authors: melo jb. Cytogenet Genome Res. 2008;121(3-4):293-7. doi: 10.1159/000138901. Epub 2008 Aug 29. Cytogenet Genome Res. 2008. PMID: 18758175

4

Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy.

Carreira IM, Melo JB, Rodrigues C, Backx L, Vermeesch J, Weise A, Kosyakova N, Oliveira G, Matoso E. Carreira IM, et al. Among authors: melo jb. Mol Cytogenet. 2009 Aug 4;2:16. doi: 10.1186/1755-8166-2-16. Mol Cytogenet. 2009. PMID: 19653912 Free PMC article.

5

Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.

Melo JB, Matoso E, Polityko A, Saraiva J, Backx L, Vermeesch JR, Kosyakova N, Ewers E, Liehr T, Carreira IM. Melo JB, et al. Cytogenet Genome Res. 2009;125(2):109-14. doi: 10.1159/000227834. Epub 2009 Aug 31. Cytogenet Genome Res. 2009. PMID: 19729913

6

Metabolic profiling of human lung cancer tissue by 1H high resolution magic angle spinning (HRMAS) NMR spectroscopy.

Rocha CM, Barros AS, Gil AM, Goodfellow BJ, Humpfer E, Spraul M, Carreira IM, Melo JB, Bernardo J, Gomes A, Sousa V, Carvalho L, Duarte IF. Rocha CM, et al. Among authors: melo jb. J Proteome Res. 2010 Jan;9(1):319-32. doi: 10.1021/pr9006574. J Proteome Res. 2010. PMID: 19908917

7

X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation.

Ferreira SI, Matoso E, Pinto M, Almeida J, Liehr T, Melo JB, Carreira IM. Ferreira SI, et al. Among authors: melo jb. Mol Cytogenet. 2010 Jul 20;3:14. doi: 10.1186/1755-8166-3-14. Mol Cytogenet. 2010. PMID: 20646274 Free PMC article.

8

Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances.

Melo JB, Backx L, Vermeesch JR, Santos HG, Sousa AC, Kosyakova N, Weise A, von Eggeling F, Liehr T, Carreira IM. Melo JB, et al. J Appl Genet. 2011 May;52(2):193-200. doi: 10.1007/s13353-011-0035-3. Epub 2011 Mar 25. J Appl Genet. 2011. PMID: 21437654 Review.

9

Critical region in 2q31.2q32.3 deletion syndrome: Report of two phenotypically distinct patients, one with an additional deletion in Alagille syndrome region.

Ferreira SI, Matoso E, Venâncio M, Saraiva J, Melo JB, Carreira IM. Ferreira SI, et al. Among authors: melo jb. Mol Cytogenet. 2012 May 2;5(1):25. doi: 10.1186/1755-8166-5-25. Mol Cytogenet. 2012. PMID: 22550961 Free PMC article.

10

Cryptic 7q36.2q36.3 deletion causes multiple congenital eye anomalies and craniofacial dysmorphism.

Beleza-Meireles A, Matoso E, Ramos L, Melo JB, Carreira IM, Silva ED, Saraiva JM. Beleza-Meireles A, et al. Among authors: melo jb. Am J Med Genet A. 2013 Mar;161A(3):589-93. doi: 10.1002/ajmg.a.35713. Epub 2013 Feb 7. Am J Med Genet A. 2013. PMID: 23401163

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