Giannotti A - Search Results

1

Intrafamilial variability of Pfeiffer-type cardiocranial syndrome.

Digilio MC, Marino B, Borzaga U, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: giannotti a. Am J Med Genet. 1997 Dec 31;73(4):480-3. Am J Med Genet. 1997. PMID: 9415478 Review.

2

Familial postaxial acrofacial dysostosis syndrome.

Giannotti A, Digilio MC, Virgili Q, Obregon MG, Guadagni AM, Ventura T, Dallapiccola B. Giannotti A, et al. J Med Genet. 1992 Oct;29(10):752. doi: 10.1136/jmg.29.10.752. J Med Genet. 1992. PMID: 1433242 Free PMC article. No abstract available.

3

Nonrandom association of atrioventricular canal and del (8p) syndrome.

Marino B, Reale A, Giannotti A, Digilio MC, Dallapiccola B. Marino B, et al. Among authors: giannotti a. Am J Med Genet. 1992 Feb 15;42(4):424-7. doi: 10.1002/ajmg.1320420404. Am J Med Genet. 1992. PMID: 1609823 Review.

4

Familial aplasia cutis congenita and coarctation of the aorta.

Dallapiccola B, Giannotti A, Marino B, Digilio C, Obregon G. Dallapiccola B, et al. Among authors: giannotti a. Am J Med Genet. 1992 Jul 1;43(4):762-3. doi: 10.1002/ajmg.1320430423. Am J Med Genet. 1992. PMID: 1621771

5

New case of Bartsocas-Papas syndrome surviving at 20 months.

Giannotti A, Digilio MC, Standoli L, Zama M, Dallapiccola B. Giannotti A, et al. Am J Med Genet. 1992 Mar 1;42(5):733-5. doi: 10.1002/ajmg.1320420522. Am J Med Genet. 1992. PMID: 1632449

6

Autosomal recessive form of whistling face syndrome in sibs.

Dallapiccola B, Giannotti A, Lembo A, Saguì L. Dallapiccola B, et al. Among authors: giannotti a. Am J Med Genet. 1989 Aug;33(4):542-4. doi: 10.1002/ajmg.1320330426. Am J Med Genet. 1989. PMID: 2596515

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: giannotti a. Am J Med Genet. 1995 Jul 3;57(3):483-8. doi: 10.1002/ajmg.1320570325. Am J Med Genet. 1995. PMID: 7677156

8

Congenital cardiac defect in a patient with mosaic 45,X/46,XX,i(21q) karyotype.

Digilio MC, Mingarelli R, Marino B, Giannotti A, Melchionda S, Dallapiccola B. Digilio MC, et al. Among authors: giannotti a. Clin Genet. 1994 Sep;46(3):268-70. doi: 10.1111/j.1399-0004.1994.tb04240.x. Clin Genet. 1994. PMID: 7820944

9

An autosomal recessive syndrome of cleft palate, cardiac defect, genital anomalies, and ectrodactyly (CCGE).

Giannotti A, Digilio MC, Mingarelli R, Dallapiccola B. Giannotti A, et al. J Med Genet. 1995 Jan;32(1):72-4. doi: 10.1136/jmg.32.1.72. J Med Genet. 1995. PMID: 7897634 Free PMC article.

10

Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum development.

Digilio MC, Giannotti A, Floridia G, Uccellatore F, Mingarelli R, Danesino C, Dallapiccola B, Zuffardi O. Digilio MC, et al. Among authors: giannotti a. J Med Genet. 1994 Mar;31(3):238-41. doi: 10.1136/jmg.31.3.238. J Med Genet. 1994. PMID: 8014974 Free PMC article.

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