Scarano G - Search Results

1

Narrowing the candidate region of Albright hereditary osteodystrophy-like syndrome by deletion mapping in a patient with an unbalanced cryptic translocation t(2;6)(q37.3;q26).

Giardino D, Finelli P, Gottardi G, De Canal G, Della Monica M, Lonardo F, Scarano G, Larizza L. Giardino D, et al. Among authors: scarano g. Am J Med Genet A. 2003 Oct 15;122A(3):261-5. doi: 10.1002/ajmg.a.20287. Am J Med Genet A. 2003. PMID: 12966529

2

CFC syndrome: report on three additional cases.

Sorge G, Di Forti F, Scarano G, Ventruto V, Zelante L, Dallapiccola B. Sorge G, et al. Among authors: scarano g. Am J Med Genet. 1989 Aug;33(4):476-8. doi: 10.1002/ajmg.1320330412. Am J Med Genet. 1989. PMID: 2596507

3

Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria.

Zollino M, Battaglia A, D'Avanzo MG, Della Bruna MM, Marini R, Scarano G, Cappa M, Neri G. Zollino M, et al. Among authors: scarano g. Am J Med Genet. 1994 Sep 1;52(3):302-7. doi: 10.1002/ajmg.1320520310. Am J Med Genet. 1994. PMID: 7810561

4

Prenatal diagnosis of femur-fibula-ulna complex by ultrasonography in a male fetus at 24 weeks of gestation.

Capece G, Fasolino A, Della Monica M, Lonardo F, Scarano G, Neri G. Capece G, et al. Among authors: scarano g. Prenat Diagn. 1994 Jun;14(6):502-5. doi: 10.1002/pd.1970140616. Prenat Diagn. 1994. PMID: 7937589

5

Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta.

Mottes M, Gomez Lira MM, Valli M, Scarano G, Lonardo F, Forlino A, Cetta G, Pignatti PF. Mottes M, et al. Among authors: scarano g. Hum Mutat. 1993;2(3):196-204. doi: 10.1002/humu.1380020308. Hum Mutat. 1993. PMID: 8364588

6

Novel findings in a patient with Weaver or a Weaver-like syndrome.

Scarano G, Della Monica M, Lonardo F, Neri G. Scarano G, et al. Am J Med Genet. 1996 May 17;63(2):378-81. doi: 10.1002/(SICI)1096-8628(19960517)63:2<378::AID-AJMG10>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8725789

7

The Williams syndrome: an Italian collaborative study.

Franceschini P, Guala A, Vardeu MP, Signorile F, Franceschini D, Mastroiacovo P, Gianotti A, Livini E, Lalatta F, Selicorni A, Andria G, Scarano G, Della Monica M, Rizzo R, Zelante L, Stabile M, Gabrielli O, Neri G. Franceschini P, et al. Among authors: scarano g. Minerva Pediatr. 1996 Oct;48(10):421-8. Minerva Pediatr. 1996. PMID: 9017917

8

Malformation syndromes with kidney dysplasia.

Genuardi M, Scarano G, Tozzi C, Chinca M, Della Monica M, Martini-Neri ME, Picardi P, Neri G. Genuardi M, et al. Among authors: scarano g. Birth Defects Orig Artic Ser. 1996;30(1):379-95. Birth Defects Orig Artic Ser. 1996. PMID: 9125343 No abstract available.

9

A case of short-rib syndrome without polydactyly in a stillborn: a new type?

Scarano G, Della Monica M, Capece G, Lonardo F, Neri G, Maroteaux P. Scarano G, et al. Birth Defects Orig Artic Ser. 1996;30(1):95-101. Birth Defects Orig Artic Ser. 1996. PMID: 9125350 No abstract available.

10

Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.

Genuardi M, Tozzi C, Pomponi MG, Stagni ML, Della Monica M, Scarano G, Calvieri F, Torrisi L, Neri G. Genuardi M, et al. Among authors: scarano g. Eur J Hum Genet. 1999 May-Jun;7(4):421-6. doi: 10.1038/sj.ejhg.5200333. Eur J Hum Genet. 1999. PMID: 10352932

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