Seuánez HN - Search Results

1

Molecular analysis of holoprosencephaly in South America.

Savastano CP, El-Jaick KB, Costa-Lima MA, Abath CM, Bianca S, Cavalcanti DP, Félix TM, Scarano G, Llerena JC Jr, Vargas FR, Moreira MÂ, Seuánez HN, Castilla EE, Orioli IM. Savastano CP, et al. Among authors: seuanez hn. Genet Mol Biol. 2014 Mar;37(1 Suppl):250-62. doi: 10.1590/s1415-47572014000200011. Genet Mol Biol. 2014. PMID: 24764759 Free PMC article.

2

Rare nasal cleft in a patient with holoprosencephaly due to a mutation in the ZIC2 gene.

Savastano CP, Bernardi P, Seuánez HN, Moreira MÂ, Orioli IM. Savastano CP, et al. Among authors: seuanez hn. Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):300-6. doi: 10.1002/bdra.23216. Epub 2014 Feb 12. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 24677696 Review.

3

Cytogenetic and molecular studies of an X;21 translocation previously diagnosed as complete monosomy 21.

Cardoso LC, Moraes L, Camilo MJ, Mulatinho MV, Ramos H, Almeida JC, Llerena JC Jr, Seuánez HN, Vargas FR. Cardoso LC, et al. Among authors: seuanez hn. Eur J Med Genet. 2008 Nov-Dec;51(6):588-97. doi: 10.1016/j.ejmg.2008.06.008. Epub 2008 Jul 12. Eur J Med Genet. 2008. PMID: 18674646

4

Constitutional and somatic methylation status of DMRH19 and KvDMR in Wilms tumor patients.

Cardoso LC, Tenorio Castaño JA, Pereira HS, Lima MA, Dos Santos AC, de Faria PS, Ferman S, Seuánez HN, Nevado JB, de Almeida JC, Lapunzina P, Vargas FR. Cardoso LC, et al. Among authors: seuanez hn. Genet Mol Biol. 2012 Dec;35(4):714-24. doi: 10.1590/S1415-47572012005000073. Epub 2012 Nov 9. Genet Mol Biol. 2012. PMID: 23271929 Free PMC article.

5

Molecular analysis of HPRT1(+) somatic cell hybrids derived from a carrier of an HPRT1 mutation responsible for Lesch-Nyhan syndrome.

Rivero MB, Olicio R, Lima CR, Bonvicino CR, Moreira MA, Llerena JC, Seuánez HN. Rivero MB, et al. Among authors: seuanez hn. Am J Med Genet. 2001 Sep 15;103(1):48-55. doi: 10.1002/ajmg.1514. Am J Med Genet. 2001. PMID: 11562934

6

Detailed analysis of X chromosome inactivation in a 49,XXXXX pentasomy.

Moraes LM, Cardoso LC, Moura VL, Moreira MA, Menezes AN, Llerena JC Jr, Seuánez HN. Moraes LM, et al. Among authors: seuanez hn. Mol Cytogenet. 2009 Oct 7;2:20. doi: 10.1186/1755-8166-2-20. Mol Cytogenet. 2009. PMID: 19811657 Free PMC article.

7

Constitutive RB1 mutation in a child conceived by in vitro fertilization: implications for genetic counseling.

Barbosa RH, Vargas FR, Lucena E, Bonvicino CR, Seuánez HN. Barbosa RH, et al. Among authors: seuanez hn. BMC Med Genet. 2009 Jul 29;10:75. doi: 10.1186/1471-2350-10-75. BMC Med Genet. 2009. PMID: 19640284 Free PMC article.

8

Family-based genome-wide association study in Patagonia confirms the association of the DMD locus and cleft lip and palate.

Fonseca RF, de Carvalho FM, Poletta FA, Montaner D, Dopazo J, Mereb JC, Moreira MAM, Seuanez HN, Vieira AR, Castilla EE, Orioli IM. Fonseca RF, et al. Among authors: seuanez hn. Eur J Oral Sci. 2015 Oct;123(5):381-384. doi: 10.1111/eos.12212. Epub 2015 Sep 1. Eur J Oral Sci. 2015. PMID: 26331285

9

Assignment of TCF1, TGM1, CALM1, CKB, THBS1, B2M, and FES in Ateles paniscus chamek (Platyrrhini, Primates).

Moreira MA, Canavez F, Parham P, Seuánez HN. Moreira MA, et al. Among authors: seuanez hn. Cytogenet Cell Genet. 1997;79(1-2):92-6. doi: 10.1159/000134690. Cytogenet Cell Genet. 1997. PMID: 9533020

10

Induction and characterization of hypoxanthine-phosphoribosyltransferase (Hprt-) deficient cell lines of Akodon cursor (Rodentia, Sigmodontinae).

Bonvicino CR, Moreira MA, Arcuri RA, Seuánez HN. Bonvicino CR, et al. Among authors: seuanez hn. Cytogenet Cell Genet. 2001;92(1-2):153-6. doi: 10.1159/000056888. Cytogenet Cell Genet. 2001. PMID: 11306816

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