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Supernumerary ring chromosome 8: clinical and molecular cytogenetic characterization in a case report.
Am J Med Genet A. 2004 Oct 15;130A(3):288-94. doi: 10.1002/ajmg.a.20677.
Am J Med Genet A. 2004.
PMID: 15378554
Review.
Trisomy 12p and monosomy 4p: phenotype-genotype correlation.
Benussi DG, Costa P, Zollino M, Murdolo M, Petix V, Carrozzi M, Pecile V.
Benussi DG, et al.
Genet Test Mol Biomarkers. 2009 Apr;13(2):199-204. doi: 10.1089/gtmb.2008.0109.
Genet Test Mol Biomarkers. 2009.
PMID: 19378504
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Ophthalmic features in a dysmorphic boy with chromosome 4q deletion and duplication.
Parentin F, Fabretto A, Benussi DG, Petix V, Marchetti F, Dalprà L, Redaelli S, Pensiero S, Pecile V.
Parentin F, et al. Among authors: benussi dg.
Ophthalmic Genet. 2009 Jun;30(2):103-5. doi: 10.1080/13816810802592559.
Ophthalmic Genet. 2009.
PMID: 19373683
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A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning.
Villa N, Conconi D, Benussi DG, Tornese G, Crosti F, Sala E, Dalprà L, Pecile V.
Villa N, et al. Among authors: benussi dg.
Mol Cytogenet. 2017 Jun 13;10:22. doi: 10.1186/s13039-017-0323-7. eCollection 2017.
Mol Cytogenet. 2017.
PMID: 28630649
Free PMC article.
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Fragile X syndrome, mental retardation and macroorchidism.
Vatta S, Cigui I, Demori E, Morgutti M, Pecile V, Benussi DG, Serra C, Amoroso A.
Vatta S, et al. Among authors: benussi dg.
Clin Genet. 1998 Oct;54(4):366-7. doi: 10.1034/j.1399-0004.1998.5440420.x.
Clin Genet. 1998.
PMID: 9831354
No abstract available.
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Prenatal diagnosis of Miller-Dieker syndrome by ultrasound and molecular cytogenetic analysis.
Lenzini E, D'Ottavio G, Città A, Benussi DG, Petix V, Pecile V.
Lenzini E, et al. Among authors: benussi dg.
Clin Genet. 2007 Nov;72(5):487-9. doi: 10.1111/j.1399-0004.2007.00830.x. Epub 2007 Sep 10.
Clin Genet. 2007.
PMID: 17850357
No abstract available.
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Different morphologic aspects and clinical features in massive hepatic amyloidosis.
Melato M, Manconi R, Magris D, Morassi P, Benussi DG, Tiribelli C.
Melato M, et al. Among authors: benussi dg.
Digestion. 1984;29(3):138-45. doi: 10.1159/000199023.
Digestion. 1984.
PMID: 6745505
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Amyloidosis of specialized mesodermal tissues in non-myelomatous monoclonal gammopathy. A pathogenetic hypothesis.
Melato M, Antonutto G, Manconi R, Benussi DG.
Melato M, et al. Among authors: benussi dg.
Pathol Res Pract. 1983 Aug;178(1):78-82. doi: 10.1016/s0344-0338(83)80089-2.
Pathol Res Pract. 1983.
PMID: 6647154
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