Divizia MT - Search Results

1

De novo deletion of chromosome 11q12.3 in monozygotic twins affected by Poland Syndrome.

Vaccari CM, Romanini MV, Musante I, Tassano E, Gimelli S, Divizia MT, Torre M, Morovic CG, Lerone M, Ravazzolo R, Puliti A. Vaccari CM, et al. Among authors: divizia mt. BMC Med Genet. 2014 May 30;15:63. doi: 10.1186/1471-2350-15-63. BMC Med Genet. 2014. PMID: 24885342 Free PMC article.

2

Auriculo-condylar syndrome or new syndrome?

Divizia MT, Cordone A, Bado M, Rosaia L, Cirillo Silengo M, Ravazzolo R, Lerone M. Divizia MT, et al. Clin Dysmorphol. 2002 Apr;11(2):143-4. doi: 10.1097/00019605-200204000-00015. Clin Dysmorphol. 2002. PMID: 12002148

3

The first intron of the human osteopontin gene contains a C/EBP-beta-responsive enhancer.

Giacopelli F, Rosatto N, Divizia MT, Cusano R, Caridi G, Ravazzolo R. Giacopelli F, et al. Among authors: divizia mt. Gene Expr. 2003;11(2):95-104. doi: 10.3727/000000003108748991. Gene Expr. 2003. PMID: 12837040 Free PMC article.

4

How wide is the ocular spectrum of Delleman syndrome?

Divizia MT, Priolo M, Priolo E, Ottonello G, Baban A, Rossi A, Silengo MC, Lerone M. Divizia MT, et al. Clin Dysmorphol. 2004 Jan;13(1):33-4. doi: 10.1097/00019605-200401000-00009. Clin Dysmorphol. 2004. PMID: 15127763

5

Unilateral radio-ulnar synostosis associated with hypotonia, developmental delay, and facial dysmorphism.

Divizia MT, Baban A, Pessagno A, Boero S, Ravazzolo R, Silengo MC, Lerone M. Divizia MT, et al. Am J Med Genet A. 2005 Aug 15;137(1):106-8. doi: 10.1002/ajmg.a.30879. Am J Med Genet A. 2005. PMID: 16015584 Review. No abstract available.

6

Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation.

Bocciardi R, Giorda R, Buttgereit J, Gimelli S, Divizia MT, Beri S, Garofalo S, Tavella S, Lerone M, Zuffardi O, Bader M, Ravazzolo R, Gimelli G. Bocciardi R, et al. Among authors: divizia mt. Hum Mutat. 2007 Jul;28(7):724-31. doi: 10.1002/humu.20511. Hum Mutat. 2007. PMID: 17373680

7

Pituitary hypoplasia and growth hormone deficiency in Coffin-Siris syndrome.

Baban A, Moresco L, Divizia MT, Rossi A, Ravazzolo R, Lerone M, De Toni T. Baban A, et al. Among authors: divizia mt. Am J Med Genet A. 2008 Feb 1;146A(3):384-8. doi: 10.1002/ajmg.a.32111. Am J Med Genet A. 2008. PMID: 18203175 No abstract available.

8

Further case of metaphyseal acroscyphodysplasia with cone-shaped epiphyses (Bellini disease or metaphyseal dyschondroplasia).

De Toni T, Baban A, Colombo E, Arnello A, Divizia MT, Lerone M. De Toni T, et al. Among authors: divizia mt. Clin Dysmorphol. 2008 Oct;17(4):275-8. doi: 10.1097/MCD.0b013e3282fc77ec. Clin Dysmorphol. 2008. PMID: 18978659 Review. No abstract available.

9

Craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis: probably a new syndrome.

Capra V, De Marco P, Merello E, Baffico AM, Baldi M, Divizia MT, Gimelli S, Mallet D, Raso A, Mascelli S, Tomà P, Rossi A, Pavanello M, Cama A, Magnani C. Capra V, et al. Among authors: divizia mt. Eur J Med Genet. 2009 Jan-Feb;52(1):17-22. doi: 10.1016/j.ejmg.2008.10.005. Epub 2008 Nov 6. Eur J Med Genet. 2009. PMID: 19022412

10

Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports.

Bernardini L, Gimelli S, Gervasini C, Carella M, Baban A, Frontino G, Barbano G, Divizia MT, Fedele L, Novelli A, Béna F, Lalatta F, Miozzo M, Dallapiccola B. Bernardini L, et al. Among authors: divizia mt. Orphanet J Rare Dis. 2009 Nov 4;4:25. doi: 10.1186/1750-1172-4-25. Orphanet J Rare Dis. 2009. PMID: 19889212 Free PMC article.

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