Copelli SB - Search Results

1

Molecular genetics of hereditary thyroid diseases due to a defect in the thyroglobulin or thyroperoxidase synthesis.

Targovnik HM, Varela V, Frechtel GD, Cerrone GE, Copelli SB, Propato FV, Mendive F. Targovnik HM, et al. Among authors: copelli sb. Braz J Med Biol Res. 1994 Dec;27(12):2745-57. Braz J Med Biol Res. 1994. PMID: 7549998 Review.

2

Molecular analysis of sex determination in sex-reversed and true hermaphroditism.

Copelli SB, Bergadá C, Billerbeck AE, Goldberg AC, Kalil J, Damiani D, Targovnik HM. Copelli SB, et al. Braz J Med Biol Res. 1996 Jun;29(6):743-8. Braz J Med Biol Res. 1996. PMID: 9070386

3

[Molecular sex determination. Significance in the diagnosis of gonadal pathologies].

Copelli S, Targovnik H, Bergada C. Copelli S, et al. Medicina (B Aires). 1995;55(6):705-11. Medicina (B Aires). 1995. PMID: 8731584 Spanish.

4

[Molecular bases of α-thalassemia in Argentina].

Scheps KG, Francipane L, Nash A, Cerrone GE, Copelli SB, Varela V. Scheps KG, et al. Among authors: copelli sb. Medicina (B Aires). 2015;75(2):81-6. Medicina (B Aires). 2015. PMID: 25919868 Free article. Spanish.

5

PCR analysis of Y-chromosome sequences in a 45,X male patient and a review of the literature.

Copelli S, Castiñeyra G, Levalle O, Aszpis S, Mormandi E, Targovnik H. Copelli S, et al. Arch Androl. 2000 Mar-Apr;44(2):137-45. doi: 10.1080/014850100262317. Arch Androl. 2000. PMID: 10746871 Review.

6

Absence of mutations in the p53 tumor suppressor gene in non-invasive Cushing adenomas.

Copelli SB, Loza Coll MA, Bruno OD. Copelli SB, et al. Medicina (B Aires). 1999;59(5 Pt 1):459-62. Medicina (B Aires). 1999. PMID: 10684166

7

Molecular characterization of a novel splice site mutation within the CYBB gene leading to X-linked chronic granulomatous disease.

Barese CN, Copelli SB, De Matteo E, Zandomeni R, Salgueiro F, Di Giovanni D, Heyworth P, Rivas EM. Barese CN, et al. Among authors: copelli sb. Pediatr Blood Cancer. 2005 Apr;44(4):420-2. doi: 10.1002/pbc.20204. Pediatr Blood Cancer. 2005. PMID: 15468310

8

Familial occurrence of the IMAGe association: additional clinical variants and a proposed mode of inheritance.

Bergadá I, Del Rey G, Lapunzina P, Bergadá C, Fellous M, Copelli S. Bergadá I, et al. J Clin Endocrinol Metab. 2005 Jun;90(6):3186-90. doi: 10.1210/jc.2004-1589. Epub 2005 Mar 15. J Clin Endocrinol Metab. 2005. PMID: 15769992 Review.

9

Partial defects in transcriptional activity of two novel DAX-1 mutations in childhood-onset adrenal hypoplasia congenita.

Laissue P, Copelli S, Bergada I, Bergada C, Barrio G, Karaboga S, Wurtz JM, Fellous M, Lalli E, Veitia RA. Laissue P, et al. Clin Endocrinol (Oxf). 2006 Nov;65(5):681-6. doi: 10.1111/j.1365-2265.2006.02649.x. Clin Endocrinol (Oxf). 2006. PMID: 17054473

10

[Molecular pathogenesis of carcinoma of the esophagus].

Giménez AM, Copelli SB, Speroni AH, Meiss RP. Giménez AM, et al. Among authors: copelli sb. Medicina (B Aires). 2003;63(3):237-48. Medicina (B Aires). 2003. PMID: 12876912 Review. Spanish.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

23 results

Search Page

Filters