Cao A - Search Results

1

A novel beta-thalassemia mutation (G-->A) at the initiation codon of the beta-globin gene.

Saba L, Meloni A, Sardu R, Travi M, Primignani P, Rosatelli MC, Cao A. Saba L, et al. Among authors: cao a. Hum Mutat. 1992;1(5):420-2. doi: 10.1002/humu.1380010512. Hum Mutat. 1992. PMID: 1301952 No abstract available.

2

A simple electrophoretic procedure for fetal diagnosis of beta-thalassaemia due to short deletions.

Faà V, Rosatelli MC, Sardu R, Meloni A, Toffoli C, Cao A. Faà V, et al. Among authors: cao a. Prenat Diagn. 1992 Nov;12(11):903-8. doi: 10.1002/pd.1970121109. Prenat Diagn. 1992. PMID: 1494543

3

Molecular characterization of beta-thalassemia in the Sardinian population.

Rosatelli MC, Dozy A, Faà V, Meloni A, Sardu R, Saba L, Kan YW, Cao A. Rosatelli MC, et al. Among authors: cao a. Am J Hum Genet. 1992 Feb;50(2):422-6. Am J Hum Genet. 1992. PMID: 1734721 Free PMC article.

4

Two novel mutations in the transmembrane domains of the CFTR gene in subjects of Sardinian descent.

Saba L, Leoni GB, Meloni A, Faà V, Cao A, Rosatelli MC. Saba L, et al. Among authors: cao a. Hum Mol Genet. 1993 Oct;2(10):1739-40. doi: 10.1093/hmg/2.10.1739. Hum Mol Genet. 1993. PMID: 7505693 No abstract available.

5

Homozygous beta-thalassaemia resulting in the beta-thalassaemia carrier state phenotype.

Rosatelli MC, Pischedda A, Meloni A, Saba L, Pomo A, Travi M, Fattore S, Cao A. Rosatelli MC, et al. Among authors: cao a. Br J Haematol. 1994 Nov;88(3):562-5. doi: 10.1111/j.1365-2141.1994.tb05074.x. Br J Haematol. 1994. PMID: 7819068

6

A novel beta-thalassemia mutation: frameshift at codon 59 detected in an Italian carrier.

Meloni A, Demurtas M, Moi L, Faà V, Cao A, Rosatelli MC. Meloni A, et al. Among authors: cao a. Hum Mutat. 1994;3(3):309-11. doi: 10.1002/humu.1380030322. Hum Mutat. 1994. PMID: 8019567 No abstract available.

7

New frameshift mutation in the DAX-1 gene in a patient with X-linked adrenal hypoplasia and hypogonadotropic hypogonadism.

Meloni A, Meloni A, Cao A, Rosatelli MC. Meloni A, et al. Among authors: cao a. Hum Mutat. 1996;8(2):183-4. doi: 10.1002/(SICI)1098-1004(1996)8:2<183::AID-HUMU12>3.0.CO;2-Z. Hum Mutat. 1996. PMID: 8844218 No abstract available.

8

Molecular diagnosis and carrier screening for beta thalassemia.

Cao A, Saba L, Galanello R, Rosatelli MC. Cao A, et al. JAMA. 1997 Oct 15;278(15):1273-7. JAMA. 1997. PMID: 9333270

9

Two novel mutations of the AIRE protein affecting its homodimerization properties.

Meloni A, Fiorillo E, Corda D, Perniola R, Cao A, Rosatelli MC. Meloni A, et al. Among authors: cao a. Hum Mutat. 2005 Mar;25(3):319. doi: 10.1002/humu.9309. Hum Mutat. 2005. PMID: 15712268

10

Screening for thalassemia: a model of success.

Cao A, Rosatelli MC, Monni G, Galanello R. Cao A, et al. Obstet Gynecol Clin North Am. 2002 Jun;29(2):305-28, vi-vii. doi: 10.1016/s0889-8545(01)00006-7. Obstet Gynecol Clin North Am. 2002. PMID: 12108831 Review.

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