Baroncini A - Search Results

1

Nasal abnormalities in the 9p deletion syndrome.

Compadretti GC, Tasca I, Baroncini A, Pittalis MC. Compadretti GC, et al. Among authors: baroncini a. Arch Otolaryngol Head Neck Surg. 2007 Oct;133(10):1054-6. doi: 10.1001/archotol.133.10.1054. Arch Otolaryngol Head Neck Surg. 2007. PMID: 17938332 No abstract available.

2

Cytogenetic follow-up of chromosomal mosaicism detected in first-trimester prenatal diagnosis.

Battaglia P, Baroncini A, Mattarozzi A, Baccolini I, Capucci A, Spada F, Pompilii E, Pittalis MC. Battaglia P, et al. Among authors: baroncini a. Prenat Diagn. 2014 Aug;34(8):739-47. doi: 10.1002/pd.4358. Epub 2014 Apr 8. Prenat Diagn. 2014. PMID: 24633594

3

FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype.

Baroncini A, Rivieri F, Capucci A, Croci G, Franchi F, Sensi A, Battaglia P, Aiello V, Calzolari E. Baroncini A, et al. Eur J Med Genet. 2005 Oct-Dec;48(4):388-96. doi: 10.1016/j.ejmg.2005.05.002. Eur J Med Genet. 2005. PMID: 16378923

4

Distal 12p deletion in a stillborn infant.

Baroncini A, Avellini C, Neri C, Forabosco A. Baroncini A, et al. Am J Med Genet. 1990 Jul;36(3):358-60. doi: 10.1002/ajmg.1320360324. Am J Med Genet. 1990. PMID: 2363438

5

Evolutionary descent of a human chromosome 6 neocentromere: a jump back to 17 million years ago.

Capozzi O, Purgato S, D'Addabbo P, Archidiacono N, Battaglia P, Baroncini A, Capucci A, Stanyon R, Della Valle G, Rocchi M. Capozzi O, et al. Among authors: baroncini a. Genome Res. 2009 May;19(5):778-84. doi: 10.1101/gr.085688.108. Genome Res. 2009. PMID: 19411601 Free PMC article.

6

Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q.

Bonaglia MC, Giorda R, Poggi G, Raggi ME, Rossi E, Baroncini A, Giglio S, Borgatti R, Zuffardi O. Bonaglia MC, et al. Among authors: baroncini a. Eur J Hum Genet. 2000 Aug;8(8):597-603. doi: 10.1038/sj.ejhg.5200509. Eur J Hum Genet. 2000. PMID: 10951522

7

Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome.

Bonaglia MC, Giorda R, Mani E, Aceti G, Anderlid BM, Baroncini A, Pramparo T, Zuffardi O. Bonaglia MC, et al. Among authors: baroncini a. J Med Genet. 2006 Oct;43(10):822-8. doi: 10.1136/jmg.2005.038604. Epub 2005 Nov 11. J Med Genet. 2006. PMID: 16284256 Free PMC article.

8

Terminal osseous dysplasia with pigmentary defects: clinical description of a new family.

Baroncini A, Castelluccio P, Morleo M, Soli F, Franco B. Baroncini A, et al. Am J Med Genet A. 2007 Jan 1;143A(1):51-7. doi: 10.1002/ajmg.a.31557. Am J Med Genet A. 2007. PMID: 17152064

9

Prenatal genetic counseling referrals for advanced maternal age: still room for improvement.

Pompilii E, Astolfi G, Calabrese O, Calzolari E, Ferlini A, Lucci M, Parmeggiani G, Seri M, Baroncini A. Pompilii E, et al. Among authors: baroncini a. Prenat Diagn. 2014 Jan;34(1):71-4. doi: 10.1002/pd.4257. Prenat Diagn. 2014. PMID: 24166136

10

Molecular and cytogenetic analysis of the spreading of X inactivation in a girl with microcephaly, mild dysmorphic features and t(X;5)(q22.1;q31.1).

Giorda R, Bonaglia MC, Milani G, Baroncini A, Spada F, Beri S, Menozzi G, Rusconi M, Zuffardi O. Giorda R, et al. Among authors: baroncini a. Eur J Hum Genet. 2008 Aug;16(8):897-905. doi: 10.1038/ejhg.2008.28. Epub 2008 Feb 27. Eur J Hum Genet. 2008. PMID: 18301446

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