Zollino M - Search Results

1

Marangi G, Leuzzi V, Manti F, Lattante S, Orteschi D, Pecile V, Neri G, Zollino M. Marangi G, et al. Among authors: zollino m. Eur J Hum Genet. 2013 Feb;21(2):229-32. doi: 10.1038/ejhg.2012.79. Epub 2012 May 2. Eur J Hum Genet. 2013. PMID: 22549410 Free PMC article.

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

Chronic myelogenous leukemia in the course of chronic lymphocytic leukemia: evidence for an independent clonal origin.

Zollino M, Genuardi M, Tanci P, Mango G, Rumi C, Mancini R, Neri G. Zollino M, et al. Leuk Res. 1991;15(4):269-73. doi: 10.1016/0145-2126(91)90130-l. Leuk Res. 1991. PMID: 2030609

6

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

7

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

8

"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

9

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

10

Partial duplication of chromosome 1q preceding the development of an L3 lymphoblastic leukemia with t(8;14), secondary to treatment for Hodgkin's disease.

Zollino M, Genuardi M, De Santis R, Leone G, Marra R, Mancini R, Mango G, Neri G. Zollino M, et al. Eur J Haematol. 1988 Mar;40(3):193-7. doi: 10.1111/j.1600-0609.1988.tb00823.x. Eur J Haematol. 1988. PMID: 3162717

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