Moreira-Filho CA - Search Results

1

Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments.

Damiani D, Guedes DR, Fellous M, Barbaux S, McElreavey K, Kalil J, Goldberg AC, Moreira-Filho CA, Barbosa A, Della Manna T, Dichtchekenian V, Setian N. Damiani D, et al. J Pediatr Endocrinol Metab. 1999 Nov-Dec;12(6):827-31. doi: 10.1515/jpem.1999.12.6.827. J Pediatr Endocrinol Metab. 1999. PMID: 10614539

2

XY gonadal dysgenesis and gonadoblastoma: a study in two sisters with a cryptic deletion of the Y chromosome involving the SRY gene.

Barbosa AS, Ferraz-Costa TE, Semer M, Liberman B, Moreira-Filho CA. Barbosa AS, et al. Hum Genet. 1995 Jan;95(1):63-6. doi: 10.1007/BF00225076. Hum Genet. 1995. PMID: 7814028

3

Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal gene.

Mendonça BB, Barbosa AS, Arnhold IJ, McElreavey K, Fellous M, Moreira-Filho CA. Mendonça BB, et al. Am J Med Genet. 1994 Aug 1;52(1):39-43. doi: 10.1002/ajmg.1320520108. Am J Med Genet. 1994. PMID: 7977459

4

The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor.

Barbosa AS, Hadjiathanasiou CG, Theodoridis C, Papathanasiou A, Tar A, Merksz M, Györvári B, Sultan C, Dumas R, Jaubert F, Niaudet P, Moreira-Filho CA, Cotinot C, Fellous M. Barbosa AS, et al. Hum Mutat. 1999;13(2):146-53. doi: 10.1002/(SICI)1098-1004(1999)13:2<146::AID-HUMU7>3.0.CO;2-I. Hum Mutat. 1999. PMID: 10094551

5

Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis.

Ottolenghi C, Moreira-Filho C, Mendonça BB, Barbieri M, Fellous M, Berkovitz GD, McElreavey K. Ottolenghi C, et al. J Clin Endocrinol Metab. 2001 Jun;86(6):2465-9. doi: 10.1210/jcem.86.6.7539. J Clin Endocrinol Metab. 2001. PMID: 11397841

6

A cost-effective screening test for detecting AZF microdeletions on the human Y chromosome.

Pieri Pde C, Pereira DH, Glina S, Hallak J, McElreavey K, Moreira-Filho CA. Pieri Pde C, et al. Genet Test. 2002 Fall;6(3):185-94. doi: 10.1089/109065702761403342. Genet Test. 2002. PMID: 12490058

7

Persistence of Müllerian remnants in complete androgen insensitivity syndrome.

Damiani D, Mascolli MA, Almeida MJ, Jaubert F, Fellous M, Dichtchekenian V, Tobo PR, Moreira-Filho CA, Setian N. Damiani D, et al. J Pediatr Endocrinol Metab. 2002 Nov-Dec;15(9):1553-6. doi: 10.1515/jpem.2002.15.9.1553. J Pediatr Endocrinol Metab. 2002. PMID: 12503865

8

Molecular characterization of a bovine Y-specific DNA sequence conserved in taurine and zebu breeds.

Alves BC, Mayer MG, Taber AP, Egito AA, Fagundes V, McElreavey K, Moreira-Filho CA. Alves BC, et al. DNA Seq. 2006 Jun;17(3):199-202. doi: 10.1080/10425170600886532. DNA Seq. 2006. PMID: 17286047

9

SRY-negative true hermaphrodites and an XX male in two generations of the same family.

Ramos ES, Moreira-Filho CA, Vicente YA, Llorach-Velludo MA, Tucci S Jr, Duarte MH, Araújo AG, Martelli L. Ramos ES, et al. Hum Genet. 1996 May;97(5):596-8. doi: 10.1007/BF02281867. Hum Genet. 1996. PMID: 8655137

10

X;Y translocation revealed by chromosome microdissection and FISH in fertile XY females in the Brazilian rodent Akodon montensis.

Fagundes V, Christoff AU, Scalzi-Martin J, Hozier J, Moreira-Filho CA, Yonenaga-Yassuda Y. Fagundes V, et al. Cytogenet Cell Genet. 2000;88(1-2):124-9. doi: 10.1159/000015504. Cytogenet Cell Genet. 2000. PMID: 10773685

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