Mammi I - Search Results

1

Mutation producing alternative splicing of exon 26 in the COL1A2 gene causes type IV osteogenesis imperfecta with intrafamilial clinical variability.

Zolezzi F, Valli M, Clementi M, Mammi I, Cetta G, Pignatti PF, Mottes M. Zolezzi F, et al. Among authors: mammi i. Am J Med Genet. 1997 Aug 22;71(3):366-70. doi: 10.1002/(sici)1096-8628(19970822)71:3<366::aid-ajmg21>3.0.co;2-h. Am J Med Genet. 1997. PMID: 9268111

2

Family with branchial arch anomalies, hearing loss, ear and commissural lip pits, and rib anomalies. A new autosomal recessive condition: branchio-oto-costal syndrome?

Clementi M, Mammi I, Tenconi R. Clementi M, et al. Among authors: mammi i. Am J Med Genet. 1997 Jan 10;68(1):91-3. Am J Med Genet. 1997. PMID: 8986284

3

Is visual field reduction a component manifestation of osteopathia striata with cranial sclerosis?

Clementi M, Bellato S, Rossetti A, Mammi I, Tenconi R. Clementi M, et al. Among authors: mammi i. Am J Med Genet. 1993 Jul 1;46(6):724-6. doi: 10.1002/ajmg.1320460626. Am J Med Genet. 1993. PMID: 8362918

4

Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involved.

Mammi I, Iles DE, Smeets D, Clementi M, Tenconi R. Mammi I, et al. Hum Genet. 1996 Sep;98(3):317-20. doi: 10.1007/s004390050214. Hum Genet. 1996. PMID: 8707301 Free article.

5

Methimazole embryopathy: delineation of the phenotype.

Clementi M, Di Gianantonio E, Pelo E, Mammi I, Basile RT, Tenconi R. Clementi M, et al. Among authors: mammi i. Am J Med Genet. 1999 Mar 5;83(1):43-6. Am J Med Genet. 1999. PMID: 10076883 Review.

6

Neurofibromatosis type 1 growth charts.

Clementi M, Milani S, Mammi I, Boni S, Monciotti C, Tenconi R. Clementi M, et al. Among authors: mammi i. Am J Med Genet. 1999 Dec 3;87(4):317-23. doi: 10.1002/(sici)1096-8628(19991203)87:4<317::aid-ajmg7>3.0.co;2-x. Am J Med Genet. 1999. PMID: 10588837

7

Clinical application of genetic polymorphism in neurofibromatosis type 1.

Clementi M, Boni S, Mammi I, Favarato M, Tenconi R. Clementi M, et al. Among authors: mammi i. Ann Genet. 1996;39(2):92-6. Ann Genet. 1996. PMID: 8766140

8

Cardiovascular anomaly in Rieger Syndrome: heterogeneity or contiguity?

Mammi I, De Giorgio P, Clementi M, Tenconi R. Mammi I, et al. Acta Ophthalmol Scand. 1998 Aug;76(4):509-12. doi: 10.1034/j.1600-0420.1998.760424.x. Acta Ophthalmol Scand. 1998. PMID: 9716345 Free article. Review.

9

Utilization of genetic counseling by parents of a child or fetus with congenital malformation in North-East Italy.

Mammi I, Basile RT, Bellato S, Belli S, Benedicenti F, Boni S, Castellan C, Clementi M, Di Gianantonio E, Petrella M, Turolla L, Tenconi R. Mammi I, et al. Am J Med Genet A. 2003 Sep 1;121A(3):214-8. doi: 10.1002/ajmg.a.20255. Am J Med Genet A. 2003. PMID: 12923860

10

Clinical anophthalmia: an epidemiological study in northeast Italy based on 368,256 consecutive births.

Clementi M, Turolla L, Mammi I, Tenconi R. Clementi M, et al. Among authors: mammi i. Teratology. 1992 Dec;46(6):551-3. doi: 10.1002/tera.1420460604. Teratology. 1992. PMID: 1290155

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