Zollino M - Search Results

1

Mother to son amplification of a small subtelomeric deletion: a new mechanism of familial recurrence in microdeletion syndromes.

Faravelli F, Murdolo M, Marangi G, Bricarelli FD, Di Rocco M, Zollino M. Faravelli F, et al. Among authors: zollino m. Am J Med Genet A. 2007 Jun 1;143A(11):1169-73. doi: 10.1002/ajmg.a.31723. Am J Med Genet A. 2007. PMID: 17480006

2

New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and pachygyria.

Zollino M, Mastroiacovo P, Zampino G, Mariotti P, Neri G. Zollino M, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):452-7. doi: 10.1002/ajmg.1320430168. Am J Med Genet. 1992. PMID: 1605225

3

Further contribution to the description of phenotypes associated with partial 4q duplication.

Zollino M, Zampino G, Torrioli G, Pomponi MG, Neri G. Zollino M, et al. Am J Med Genet. 1995 May 22;57(1):69-73. doi: 10.1002/ajmg.1320570116. Am J Med Genet. 1995. PMID: 7645603 Review.

4

Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria.

Zollino M, Battaglia A, D'Avanzo MG, Della Bruna MM, Marini R, Scarano G, Cappa M, Neri G. Zollino M, et al. Am J Med Genet. 1994 Sep 1;52(3):302-7. doi: 10.1002/ajmg.1320520310. Am J Med Genet. 1994. PMID: 7810561

5

Costello syndrome: further clinical delineation, natural history, genetic definition, and nosology.

Zampino G, Mastroiacovo P, Ricci R, Zollino M, Segni G, Martini-Neri ME, Neri G. Zampino G, et al. Among authors: zollino m. Am J Med Genet. 1993 Aug 15;47(2):176-83. doi: 10.1002/ajmg.1320470210. Am J Med Genet. 1993. PMID: 8213903 Review.

6

More on the Noonan-CFC controversy.

Neri G, Zollino M. Neri G, et al. Among authors: zollino m. Am J Med Genet. 1996 Oct 16;65(2):100. doi: 10.1002/(SICI)1096-8628(19961016)65:2<100::AID-AJMG2>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8911597 No abstract available.

7

From Pitt-Rogers-Danks syndrome to Wolf-Hirschhorn syndrome and back?

Zollino M, Bova R, Neri G. Zollino M, et al. Am J Med Genet. 1996 Dec 2;66(1):113-5. doi: 10.1002/(SICI)1096-8628(19961202)66:1<113::AID-AJMG29>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8957527

8

"Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype.

Zollino M, Wright TJ, Di Stefano C, Tosolini A, Battaglia A, Altherr MR, Neri G. Zollino M, et al. Am J Med Genet. 1999 Feb 19;82(5):371-5. Am J Med Genet. 1999. PMID: 10069706

9

Partial duplication of the long arm of chromosome 15: confirmation of a causative role in craniosynostosis and definition of a 15q25-qter trisomy syndrome.

Zollino M, Tiziano F, Di Stefano C, Neri G. Zollino M, et al. Am J Med Genet. 1999 Dec 22;87(5):391-4. doi: 10.1002/(sici)1096-8628(19991222)87:5<391::aid-ajmg4>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10594876

10

Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome.

Zollino M, Di Stefano C, Zampino G, Mastroiacovo P, Wright TJ, Sorge G, Selicorni A, Tenconi R, Zappalà A, Battaglia A, Di Rocco M, Palka G, Pallotta R, Altherr MR, Neri G. Zollino M, et al. Am J Med Genet. 2000 Sep 18;94(3):254-61. doi: 10.1002/1096-8628(20000918)94:3<254::aid-ajmg13>3.0.co;2-7. Am J Med Genet. 2000. PMID: 10995514

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