Bertini V - Search Results

1

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. Among authors: bertini v. 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

2

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. Among authors: bertini v. 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

3

A 17q duplication prenatally detected.

Bruno R, Valetto A, Bertini V, Cosini C, Toschi B, Congregati C, Rossi S, Simi P. Bruno R, et al. Among authors: bertini v. Taiwan J Obstet Gynecol. 2015 Jun;54(3):326-9. doi: 10.1016/j.tjog.2014.05.008. Taiwan J Obstet Gynecol. 2015. PMID: 26166353 Free article. No abstract available.

4

3p26.3 terminal deletions: a challenge for prenatal genetic counseling.

Bertini V, Azzarà A, Toschi B, Gana S, Valetto A. Bertini V, et al. Prenat Diagn. 2017 Feb;37(2):197-200. doi: 10.1002/pd.4978. Epub 2017 Jan 30. Prenat Diagn. 2017. PMID: 27933663 No abstract available.

5

Next generation sequencing technologies for a successful diagnosis in a cold case of Leigh syndrome.

Aretini P, Mazzanti CM, La Ferla M, Franceschi S, Lessi F, De Gregorio V, Nesti C, Valetto A, Bertini V, Toschi B, Battini R, Caligo MA. Aretini P, et al. Among authors: bertini v. BMC Neurol. 2018 Jul 20;18(1):99. doi: 10.1186/s12883-018-1103-7. BMC Neurol. 2018. PMID: 30029642 Free PMC article.

6

17q12 microduplications: a challenge for clinicians.

Bertini V, Orsini A, Bonuccelli A, Cambi F, Del Pistoia M, Vannozzi I, Toschi B, Saggese G, Simi P, Valetto A. Bertini V, et al. Am J Med Genet A. 2015 Mar;167A(3):674-6. doi: 10.1002/ajmg.a.36905. Am J Med Genet A. 2015. PMID: 25691423

7

Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic man.

Valetto A, Bertini V, Rapalini E, Baldinotti F, Di Martino D, Simi P. Valetto A, et al. Among authors: bertini v. Fertil Steril. 2004 May;81(5):1388-90. doi: 10.1016/j.fertnstert.2003.09.069. Fertil Steril. 2004. PMID: 15136108 Free article.

8

Isolated 6q terminal deletions: an emerging new syndrome.

Bertini V, De Vito G, Costa R, Simi P, Valetto A. Bertini V, et al. Am J Med Genet A. 2006 Jan 1;140(1):74-81. doi: 10.1002/ajmg.a.31020. Am J Med Genet A. 2006. PMID: 16329114

9

Mosaic ring Y chromosome in two normal healthy men with azoospermia.

Bertini V, Canale D, Bicocchi MP, Simi P, Valetto A. Bertini V, et al. Fertil Steril. 2005 Dec;84(6):1744. doi: 10.1016/j.fertnstert.2005.06.034. Fertil Steril. 2005. PMID: 16359976 Free article.

10

Cytogenetic study of 435 subfertile men: incidence and clinical features.

Bertini V, Simi P, Valetto A. Bertini V, et al. J Reprod Med. 2006 Jan;51(1):15-20. J Reprod Med. 2006. PMID: 16482771

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