Fogu G - Search Results

1

Familial trisomy 6p in mother and daughter.

Savarese M, Grandone A, Perone L, Blanco Fdel V, De Luca G, Di Fruscio G, Fogu G, Piluso G, Perrone L, del Giudice EM, Nigro V. Savarese M, et al. Among authors: fogu g. Am J Med Genet A. 2013 Jul;161A(7):1675-81. doi: 10.1002/ajmg.a.35928. Epub 2013 May 17. Am J Med Genet A. 2013. PMID: 23687068

2

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

3

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

4

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.

5

[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.

6

Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability.

Pezzolo A, Gimelli G, Cohen A, Lavaggetto A, Romano C, Fogu G, Zuffardi O. Pezzolo A, et al. Among authors: fogu g. Hum Genet. 1993 Aug;92(1):23-7. doi: 10.1007/BF00216140. Hum Genet. 1993. PMID: 8365723

7

[The gene-dose effect for peptidase A on the erythrocytes of a patient with Edwards' syndrome].

Spano B, Balata A, Sanna MG, Fogu G, Angius AG, Sanna R, Congiu AM. Spano B, et al. Among authors: fogu g. Pediatr Med Chir. 1990 Jul-Aug;12(4):393-4. Pediatr Med Chir. 1990. PMID: 2075105 Italian.

8

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.

9

[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.

10

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.

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