Mingarelli R - Search Results

1

The link between cytogenetics and mendelism.

Dallapiccola B, Mingarelli R, Novelli G. Dallapiccola B, et al. Among authors: mingarelli r. Biomed Pharmacother. 1995;49(2):83-93. doi: 10.1016/0753-3322(96)82592-3. Biomed Pharmacother. 1995. PMID: 7605907 Review.

2

[Current advances in the cytogenetics and molecular biology of the diagnosis of malformation syndromes].

Dallapiccola B, Mingarelli R, Zelante L. Dallapiccola B, et al. Among authors: mingarelli r. Pediatr Med Chir. 1993 May-Jun;15 Suppl 1:10-3. Pediatr Med Chir. 1993. PMID: 8415186 Review. Italian.

3

Recurrent triploidy of maternal origin.

Brancati F, Mingarelli R, Dallapiccola B. Brancati F, et al. Among authors: mingarelli r. Eur J Hum Genet. 2003 Dec;11(12):972-4. doi: 10.1038/sj.ejhg.5201076. Eur J Hum Genet. 2003. PMID: 14508508

4

Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.

Obregon MG, Mingarelli R, Digilio MC, Zelante L, Giannotti A, Sabatino G, Dallapiccola B. Obregon MG, et al. Among authors: mingarelli r. Ann Genet. 1992;35(4):208-12. Ann Genet. 1992. PMID: 1296516

5

Partial deletion 10p syndrome. Report of two patients.

Obregon MG, Mingarelli R, Giannotti A, di Comite A, Spedicato FS, Dallapiccola B. Obregon MG, et al. Among authors: mingarelli r. Ann Genet. 1992;35(2):101-4. Ann Genet. 1992. PMID: 1524405

6

Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome.

Mari A, Amati F, Mingarelli R, Giannotti A, Sebastio G, Colloridi V, Novelli G, Dallapiccola B. Mari A, et al. Among authors: mingarelli r. Hum Genet. 1995 Oct;96(4):444-8. doi: 10.1007/BF00191804. Hum Genet. 1995. PMID: 7557968

7

Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): exclusion from the critical region on 8p.

Amati F, Mari A, Mingarelli R, Gennarelli M, Digilio MC, Giannotti A, Marino B, Novelli G, Dallapiccola B. Amati F, et al. Among authors: mingarelli r. Am J Med Genet. 1995 Jul 3;57(3):483-8. doi: 10.1002/ajmg.1320570325. Am J Med Genet. 1995. PMID: 7677156

8

Hypoparathyroidism as the major manifestation in two patients with 22q11 deletions.

Scirè G, Dallapiccola B, Iannetti P, Bonaiuto F, Galasso C, Mingarelli R, Boscherini B. Scirè G, et al. Among authors: mingarelli r. Am J Med Genet. 1994 Oct 1;52(4):478-82. doi: 10.1002/ajmg.1320520415. Am J Med Genet. 1994. PMID: 7747762

9

22q11 deletions in isolated and syndromic patients with tetralogy of Fallot.

Amati F, Mari A, Digilio MC, Mingarelli R, Marino B, Giannotti A, Novelli G, Dallapiccola B. Amati F, et al. Among authors: mingarelli r. Hum Genet. 1995 May;95(5):479-82. doi: 10.1007/BF00223856. Hum Genet. 1995. PMID: 7759065

10

Transposition of the great arteries associated with deletion of chromosome 22q11.

Melchionda S, Digilio MC, Mingarelli R, Novelli G, Scambler P, Marino B, Dallapiccola B. Melchionda S, et al. Among authors: mingarelli r. Am J Cardiol. 1995 Jan 1;75(1):95-8. doi: 10.1016/s0002-9149(99)80541-4. Am J Cardiol. 1995. PMID: 7801879 No abstract available.

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