Selicorni A - Search Results

1

14q32.3-qter trisomic segment: a case report and literature review.

Villa N, Scatigno A, Redaelli S, Conconi D, Cianci P, Farina C, Fossati C, Dalprà L, Maitz S, Selicorni A. Villa N, et al. Among authors: selicorni a. Mol Cytogenet. 2016 Aug 5;9:60. doi: 10.1186/s13039-016-0265-5. eCollection 2016. Mol Cytogenet. 2016. PMID: 27499811 Free PMC article.

2

Genotype-phenotype correlation in two sets of monozygotic twins with Williams syndrome.

Castorina P, Selicorni A, Bedeschi F, Dalprà L, Larizza L. Castorina P, et al. Among authors: selicorni a. Am J Med Genet. 1997 Mar 3;69(1):107-11. doi: 10.1002/(sici)1096-8628(19970303)69:1<107::aid-ajmg21>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9066894

3

A 12.4 Mb duplication of 17q11.2q12 in a patient with psychomotor developmental delay and minor anomalies.

Caselli R, Ballarati L, Selicorni A, Milani D, Maitz S, Valtorta C, Larizza L, Giardino D. Caselli R, et al. Among authors: selicorni a. Eur J Med Genet. 2010 Sep-Oct;53(5):325-8. doi: 10.1016/j.ejmg.2010.05.004. Epub 2010 Jun 2. Eur J Med Genet. 2010. PMID: 20621612

4

Genotype-phenotype correlations in a new case of 8p23.1 deletion and review of the literature.

Ballarati L, Cereda A, Caselli R, Selicorni A, Recalcati MP, Maitz S, Finelli P, Larizza L, Giardino D. Ballarati L, et al. Among authors: selicorni a. Eur J Med Genet. 2011 Jan-Feb;54(1):55-9. doi: 10.1016/j.ejmg.2010.10.003. Epub 2010 Oct 20. Eur J Med Genet. 2011. PMID: 20969981 Review.

5

Deletion of the AP1S2 gene in a child with psychomotor delay and hypotonia.

Ballarati L, Cereda A, Caselli R, Maitz S, Russo S, Selicorni A, Larizza L, Giardino D. Ballarati L, et al. Among authors: selicorni a. Eur J Med Genet. 2012 Feb;55(2):124-7. doi: 10.1016/j.ejmg.2011.12.001. Epub 2011 Dec 17. Eur J Med Genet. 2012. PMID: 22210230 Free article.

6

The association of neural axis and craniovertebral junction anomalies with scoliosis in Rubinstein-Taybi syndrome.

Giussani C, Selicorni A, Fossati C, Ingelmo P, Canonico F, Landi A, Trezza A, Riva M, Sganzerla EP. Giussani C, et al. Among authors: selicorni a. Childs Nerv Syst. 2012 Dec;28(12):2163-8. doi: 10.1007/s00381-012-1893-7. Epub 2012 Aug 23. Childs Nerv Syst. 2012. PMID: 22914921

7

Omphalocele in a patient with Noonan syndrome.

Longoni L, D'Apolito V, Cianci P, Selicorni A. Longoni L, et al. Among authors: selicorni a. Clin Dysmorphol. 2012 Oct;21(4):215-217. doi: 10.1097/MCD.0b013e3283590a5a. Clin Dysmorphol. 2012. PMID: 22932443 No abstract available.

8

First evidence of vertical paternal transmission of osteopatia striata with cranial sclerosis.

Ciceri S, Cattaneo E, Fossati C, Radice P, Selicorni A, Perotti D. Ciceri S, et al. Among authors: selicorni a. Am J Med Genet A. 2013 May;161A(5):1173-6. doi: 10.1002/ajmg.a.35813. Epub 2013 Mar 13. Am J Med Genet A. 2013. PMID: 23494899 No abstract available.

9

A boy with Burkitt lymphoma associated with Noonan syndrome due to a mutation in RAF1.

Cianci P, Tono V, Sala A, Locatelli L, Carta C, Rizzari C, Biondi A, Selicorni A. Cianci P, et al. Among authors: selicorni a. Am J Med Genet A. 2013 Jun;161A(6):1401-4. doi: 10.1002/ajmg.a.35875. Epub 2013 Apr 23. Am J Med Genet A. 2013. PMID: 23613113

10

Two cases of hepatic adenomas in patients with Wolf-Hirschhorn syndrome: a new rare complication?

Prunotto G, Cianci P, Cereda A, Scatigno A, Fossati C, Maitz S, Biondi A, Selicorni A. Prunotto G, et al. Among authors: selicorni a. Am J Med Genet A. 2013 Jul;161A(7):1759-62. doi: 10.1002/ajmg.a.35966. Epub 2013 May 21. Am J Med Genet A. 2013. PMID: 23696331

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