Scarano G - Search Results

1

Prenatal ultrasound diagnosis of a case of Pfeiffer syndrome without cloverleaf skull and review of the literature.

Nazzaro A, Della Monica M, Lonardo F, Di Blasi A, Baffico M, Baldi M, Nazzaro G, De Placido G, Scarano G. Nazzaro A, et al. Among authors: scarano g. Prenat Diagn. 2004 Nov;24(11):918-22. doi: 10.1002/pd.844. Prenat Diagn. 2004. PMID: 15565658 Review.

2

[Poland-Moebius syndrome. Description of a new case].

Scarano G, Sacco R, Lonardo F, Alfano A, Ventruto V. Scarano G, et al. Pediatr Med Chir. 1986 Jan-Feb;8(1):111-2. Pediatr Med Chir. 1986. PMID: 3014448 Italian.

3

Social and geographical inequalities in prenatal care in Italy.

Corchia C, Mastroiacovo P, Lanni R, Grimaldi V, Scarano G, Baronciani D. Corchia C, et al. Among authors: scarano g. Prenat Diagn. 1995 Jun;15(6):535-40. doi: 10.1002/pd.1970150606. Prenat Diagn. 1995. PMID: 7659687

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

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

6

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.

7

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

8

A family with X-linked recessive fusion of metacarpals IV and V.

Lonardo F, Della Monica M, Riccardi G, Riccio I, Riccio V, Scarano G. Lonardo F, et al. Among authors: scarano g. Am J Med Genet A. 2004 Feb 1;124A(4):407-10. doi: 10.1002/ajmg.a.20382. Am J Med Genet A. 2004. PMID: 14735591

9

Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndrome.

Gurrieri F, Scarano G, Garavelli L, Della Monica M, Lonardo F, Cuda D, Banchini G, Opitz JM, Neri G. Gurrieri F, et al. Among authors: scarano g. Am J Med Genet A. 2004 Apr 15;126A(2):204-7. doi: 10.1002/ajmg.a.20575. Am J Med Genet A. 2004. PMID: 15057987

10

Prenatal ultrasound diagnosis of cloacal exstrophy associated with myelocystocele complex by the 'elephant trunk-like' image and review of the literature.

Della Monica M, Nazzaro A, Lonardo F, Ferrara G, Di Blasi A, Scarano G. Della Monica M, et al. Among authors: scarano g. Prenat Diagn. 2005 May;25(5):394-7. doi: 10.1002/pd.1146. Prenat Diagn. 2005. PMID: 15909284

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