Zollino M - Search Results

1

Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome.

Garavelli L, Donadio A, Zanacca C, Banchini G, Della Giustina E, Bertani G, Albertini G, Del Rossi C, Zweier C, Rauch A, Zollino M, Neri G. Garavelli L, et al. Among authors: zollino m. Am J Med Genet A. 2003 Feb 1;116A(4):385-8. doi: 10.1002/ajmg.a.10855. Am J Med Genet A. 2003. PMID: 12522797 No abstract available.

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

The Noonan-CFC controversy.

Neri G, Zollino M, Reynolds JF. Neri G, et al. Among authors: zollino m. Am J Med Genet. 1991 Jun 1;39(3):367-70. doi: 10.1002/ajmg.1320390323. Am J Med Genet. 1991. PMID: 1867292

4

X-linked mental retardation with marfanoid habitus: first report of four Italian patients.

Lalatta F, Livini E, Selicorni A, Briscioli V, Vita A, Lugo F, Zollino M, Gurrieri F, Neri G. Lalatta F, et al. Among authors: zollino m. Am J Med Genet. 1991 Feb-Mar;38(2-3):228-32. doi: 10.1002/ajmg.1320380211. Am J Med Genet. 1991. PMID: 2018063

5

Brachy/ectrodactyly and absence or hypoplasia of the fibula: an autosomal dominant condition with low penetrance and variable expressivity.

Genuardi M, Zollino M, Bellussi A, Fuhrmann W, Neri G. Genuardi M, et al. Among authors: zollino m. Clin Genet. 1990 Nov;38(5):321-6. doi: 10.1111/j.1399-0004.1990.tb03589.x. Clin Genet. 1990. PMID: 2178076

6

Differential expression of FRA16B in peripheral lymphocytes and bone marrow cells.

Zollino M, Genuardi M, Neri G. Zollino M, et al. Cancer Genet Cytogenet. 1990 Oct 15;49(2):229-33. doi: 10.1016/0165-4608(90)90146-2. Cancer Genet Cytogenet. 1990. PMID: 2208058

7

"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatment.

Lalatta F, Clerici Bagozzi D, Salmoiraghi MG, Tagliabue P, Tischer C, Zollino M, Di Rocco C, Neri G, Opitz JM. Lalatta F, et al. Among authors: zollino m. Am J Med Genet. 1990 Dec;37(4):451-6. doi: 10.1002/ajmg.1320370404. Am J Med Genet. 1990. PMID: 2260586

8

Protective effect of S-adenosylmethionine against the induction of chromosome fragile sites.

Zollino M, Neri G. Zollino M, et al. Acta Haematol. 1987;78 Suppl 1:100-3. doi: 10.1159/000205912. Acta Haematol. 1987. PMID: 2963477

9

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.

10

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

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