Clementi M - Search Results

1

Reciprocal translocation associated with multiple exostoses in seven members of a three generation family and discovered through an infertile male.

Pramparo T, Gregato G, De Gregori M, Friso A, Clementi M, Ardenghi P, Rocchi M, Zuffardi O, Tenconi R. Pramparo T, et al. Among authors: clementi m. Am J Med Genet A. 2003 Nov 15;123A(1):79-83. doi: 10.1002/ajmg.a.20498. Am J Med Genet A. 2003. PMID: 14556251

2

Familial congenital bicuspid aortic valve: a disorder of uncertain inheritance.

Clementi M, Notari L, Borghi A, Tenconi R. Clementi M, et al. Am J Med Genet. 1996 Apr 24;62(4):336-8. doi: 10.1002/(SICI)1096-8628(19960424)62:4<336::AID-AJMG2>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8723060

3

Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndrome.

Clementi M, Tenconi R, Turolla L, Silvan C, Bortotto L, Artifoni L. Clementi M, et al. Am J Med Genet. 1991 Nov 1;41(2):246-50. doi: 10.1002/ajmg.1320410223. Am J Med Genet. 1991. PMID: 1785643

4

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. Am J Med Genet. 1997 Jan 10;68(1):91-3. Am J Med Genet. 1997. PMID: 8986284

5

Theoretical recurrence risks for cleft lip derived from a population of consecutive newborns.

Tenconi R, Clementi M, Turolla L. Tenconi R, et al. Among authors: clementi m. J Med Genet. 1988 Apr;25(4):243-6. doi: 10.1136/jmg.25.4.243. J Med Genet. 1988. PMID: 3367349 Free PMC article.

6

Uncommon Alu-mediated NF1 microdeletion with a breakpoint inside the NF1 gene.

Gervasini C, Venturin M, Orzan F, Friso A, Clementi M, Tenconi R, Larizza L, Riva P. Gervasini C, et al. Among authors: clementi m. Genomics. 2005 Feb;85(2):273-9. doi: 10.1016/j.ygeno.2004.10.014. Genomics. 2005. PMID: 15676286

7

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. Among authors: clementi m. 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

8

D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p).

Minelli A, Floridia G, Rossi E, Clementi M, Tenconi R, Camurri L, Bernardi F, Hoeller H, Previde Re C, Maraschio P, et al. Minelli A, et al. Among authors: clementi m. Hum Genet. 1993 Oct;92(4):391-6. doi: 10.1007/BF01247342. Hum Genet. 1993. PMID: 7901142

9

Neurofibromatosis type 1 growth charts.

Clementi M, Milani S, Mammi I, Boni S, Monciotti C, Tenconi R. Clementi M, et al. 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

10

Linkage analysis of neurofibromatosis type 1. Study of a homogeneous North Italian population with five DNA markers of chromosome 17.

Clementi M, Murgia A, Anglani F, Tenconi R, Turolla L, Picci L, Zacchello F. Clementi M, et al. Hum Genet. 1991 May;87(1):91-4. doi: 10.1007/BF01213101. Hum Genet. 1991. PMID: 1674720

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