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Phenotypic heterogeneity in 22q11.2 deletion syndrome: Copy Number Variants as genetic modifiers for congenital heart disease in a Brazilian cohort.
Published in:
American Journal of Medical Genetics. Part A, 2023, v. 191, n. 5, p. 1273, doi. 10.1002/ajmg.a.63145
By:
- Zamariolli, M.;
- Dantas, A. G.;
- Nunes, N.;
- Moysés‐Oliveira, M.;
- Sgardioli, I. C.;
- Soares, D. C. Q.;
- Gil‐Da‐Silva‐Lopes, V. L.;
- Kim, C. A.;
- Melaragno, M. I.
Publication type:
Article
Lymphocyte proliferation and sister chromatid exchange in Alzheimer's disease.
Published in:
1991
By:
- Melaragno, Maria Isabel;
- de Arruda Cardoso Smith, Marilia;
- Kormann-Bortolotto, Maria Helena;
- Neto, João Toniolo;
- Melaragno, M I;
- Smith, M de A;
- Kormann-Bortolotto, M H;
- Toniolo Neto, J T
Publication type:
journal article
Clinical, Cytogenetic and Molecular Study in a Case of r(3) with 3p Deletion and Review of the Literature.
Published in:
Cytogenetic & Genome Research, 2011, v. 134, n. 4, p. 325, doi. 10.1159/000329478
By:
- Guilherme, R. Santos;
- Bragagnolo, S.;
- Pellegrino, R.;
- Christofolini, D. M.;
- Takeno, S. S.;
- Carvolheira, G. M.;
- Kulikowski, L. Domenici;
- Melaragno, M. I.
Publication type:
Article
Intellectual, adaptive and behavioural characteristics in four patients with 18p deletion syndrome.
Published in:
Journal of Intellectual Disability Research, 2019, v. 63, n. 3, p. 225, doi. 10.1111/jir.12568
By:
- Mello, C. B.;
- Bueno, O. F. A.;
- Benedetto, L. M.;
- Pimenta, L. S. E.;
- Takeno, S. S.;
- Melaragno, M. I.;
- Meloni, V. A.
Publication type:
Article
Subtelomeric rearrangements and copy number variations in people with intellectual disabilities.
Published in:
Journal of Intellectual Disability Research, 2010, v. 54, n. 10, p. 938, doi. 10.1111/j.1365-2788.2010.01325.x
By:
- Christofolini, D. M.;
- De Paula Ramos, M. A.;
- Kulikowski, L. D.;
- Da Silva Bellucco, F. T.;
- Belangero, S. I. N.;
- Brunoni, D.;
- Melaragno, M. I.
Publication type:
Article

Found: 5

Phenotypic heterogeneity in 22q11.2 deletion syndrome: Copy Number Variants as genetic modifiers for congenital heart disease in a Brazilian cohort.

Lymphocyte proliferation and sister chromatid exchange in Alzheimer's disease.

Clinical, Cytogenetic and Molecular Study in a Case of r(3) with 3p Deletion and Review of the Literature.

Intellectual, adaptive and behavioural characteristics in four patients with 18p deletion syndrome.

Subtelomeric rearrangements and copy number variations in people with intellectual disabilities.