Fogu G - Search Results

1

Unbalanced 1q whole-arm translocation resulting in der(14)t(1;14)(q11-12;p11) in myelodysplastic syndrome.

Fogu G, Campus PM, Cambosu F, Moro MA, Sanna R, Fozza C, Nieddu RM, Longinotti M, Montella A. Fogu G, et al. Cytogenet Genome Res. 2012;136(4):256-63. doi: 10.1159/000338437. Epub 2012 May 10. Cytogenet Genome Res. 2012. PMID: 22571950 Review.

2

Partial trisomy of the long arm of chromosome 1: prenatal diagnosis, clinical evaluation and cytogenetic findings. Case report and review of the literature.

Cambosu F, Capobianco G, Fogu G, Bandiera P, Pirino A, Moro MA, Sanna R, Soro G, Dessole M, Montella A. Cambosu F, et al. Among authors: fogu g. J Obstet Gynaecol Res. 2013 Feb;39(2):592-7. doi: 10.1111/j.1447-0756.2012.01986.x. Epub 2012 Aug 26. J Obstet Gynaecol Res. 2013. PMID: 22925348 Review.

3

Pure partial trisomy of 6p12.1-p22.1 secondary to a familial 12/6 insertion in two malformed babies.

Fogu G, Bandiera P, Cambosu F, Carta AR, Pilo L, Serra G, Soro G, Tondi M, Tusacciu G, Montella A. Fogu G, et al. Eur J Med Genet. 2007 Mar-Apr;50(2):103-11. doi: 10.1016/j.ejmg.2006.11.002. Epub 2006 Nov 23. Eur J Med Genet. 2007. PMID: 17185054

4

Patau syndrome with long survival in a case of unusual mosaic trisomy 13.

Fogu G, Maserati E, Cambosu F, Moro MA, Poddie F, Soro G, Bandiera P, Serra G, Tusacciu G, Sanna G, Mazzarello V, Montella A. Fogu G, et al. Eur J Med Genet. 2008 Jul-Aug;51(4):303-14. doi: 10.1016/j.ejmg.2008.03.004. Epub 2008 Apr 9. Eur J Med Genet. 2008. PMID: 18495567

5

Prenatal diagnosis and molecular cytogenetic characterisation of a de novo 18p deletion.

Fogu G, Capobianco G, Cambosu F, Bandiera P, Pirino A, Moro MA, Campus PM, Soro G, Dessole M, Montella A. Fogu G, et al. J Obstet Gynaecol. 2014 Feb;34(2):192-3. doi: 10.3109/01443615.2013.834300. J Obstet Gynaecol. 2014. PMID: 24456448 Free article. No abstract available.

6

[Gene-dosage effect of esterase D enzyme on erythrocytes in a patient with Patau's syndrome].

Spano B, Fogu G, Sanna R, Angius AG, Campus PM, Cattina A, Chiarolini A, Olzai MG, Balata A. Spano B, et al. Among authors: fogu g. Pediatr Med Chir. 1990 Jan-Feb;12(1):67-9. Pediatr Med Chir. 1990. PMID: 2377566 Italian.

7

[Trisomy 18: phenotypic and biochemical variability].

Fogu G, Spano B, Sanna R, Angius AG, Campus PM, Olzai MG, Sanna MG, Balata A, Chiarolini A. Fogu G, et al. Pediatr Med Chir. 1991 Jul-Aug;13(4):397-8. Pediatr Med Chir. 1991. PMID: 1754474 Italian.

8

Identification of a mutant allele of the androgen receptor gene in a family with androgen insensitivity syndrome: detection of carriers and prenatal diagnosis.

Fogu G, Bertini V, Dessole S, Bandiera P, Campus PM, Capobianco G, Sanna R, Soro G, Montella A. Fogu G, et al. Arch Gynecol Obstet. 2003 Nov;269(1):25-9. doi: 10.1007/s00404-002-0386-4. Epub 2003 Mar 20. Arch Gynecol Obstet. 2003. PMID: 14605819

9

Genotoxic effects of cadmium chloride on human amniotic fluid cells cultured in vitro.

Fogu G, Congiu AM, Campus PM, Ladu R, Sanna R, Sini MC, Soro G. Fogu G, et al. Ann Chim. 2000 Nov-Dec;90(11-12):709-14. Ann Chim. 2000. PMID: 11218258

10

Identification of a mutant allele of the androgen receptor gene in a family with androgen insensitivity syndrome: detection of carriers and prenatal diagnosis.

Fogu G, Bertini V, Dessole S, Bandiera P, Campus PM, Capobianco G, Sanna R, Soro G, Montella A. Fogu G, et al. Arch Gynecol Obstet. 2004 May;269(4):266-9. doi: 10.1007/s00404-002-0405-5. Epub 2003 Jul 31. Arch Gynecol Obstet. 2004. PMID: 12898143

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