Ceratto N - Search Results

1

Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304.

Goonewardena P, Brown WT, Gross AC, Ferrando C, Dobkin C, Romano V, Bosco P, Ceratto N, Pettersson U, Dahl N. Goonewardena P, et al. Among authors: ceratto n. Am J Med Genet. 1991 Feb-Mar;38(2-3):322-7. doi: 10.1002/ajmg.1320380231. Am J Med Genet. 1991. PMID: 1673305

2

Human type I cytokeratin genes are a compact cluster.

Ceratto N, Dobkin C, Carter M, Jenkins E, Yao XL, Cassiman JJ, Aly MS, Bosco P, Leube R, Langbein L, Feo S, Romano V. Ceratto N, et al. Cytogenet Cell Genet. 1997;77(3-4):169-74. doi: 10.1159/000134566. Cytogenet Cell Genet. 1997. PMID: 9284906

3

Preliminary studies on the molecular basis of hyperphenylalaninemia in Egypt.

Hashem N, Bosco P, Chiavetta V, Calì F, Ceratto N, Romano V. Hashem N, et al. Among authors: ceratto n. Hum Genet. 1996 Jul;98(1):3-6. doi: 10.1007/s004390050150. Hum Genet. 1996. PMID: 8682503

4

RFLP discordance in a PKU family due to a deletion in the PAH gene.

Bosco P, Ceratto N, Cali F, Goltsov AA, Eisensmith RC, Novelli G, Dalla Piccola B, Romano V. Bosco P, et al. Among authors: ceratto n. Turk J Pediatr. 1996 Oct-Dec;38(4):497-504. Turk J Pediatr. 1996. PMID: 8993180

5

Two novel PAH gene mutations detected in Italian phenylketonuric patients.

Argiolas A, Bosco P, Calì F, Ceratto N, Anello G, Riva E, Biasucci G, Carducci C, Romano V. Argiolas A, et al. Among authors: ceratto n. Hum Genet. 1997 Feb;99(2):275-8. doi: 10.1007/s004390050353. Hum Genet. 1997. PMID: 9048935

6

Identification of two new phenylalanine hydroxylase alleles in Sicilian phenylketonuric families.

Romano V, Ceratto N, Chiavetta V, Bosco P. Romano V, et al. Among authors: ceratto n. J Inherit Metab Dis. 1993;16(3):599-601. doi: 10.1007/BF00711692. J Inherit Metab Dis. 1993. PMID: 7609461 No abstract available.

7

Prenatal diagnosis by minisatellite analysis in Italian families with phenylketonuria.

Romano V, Dianzani I, Ponzone A, Zammarchi E, Eisensmith R, Ceratto N, Bosco P, Indelicato A. Romano V, et al. Among authors: ceratto n. Prenat Diagn. 1994 Oct;14(10):959-62. doi: 10.1002/pd.1970141011. Prenat Diagn. 1994. PMID: 7899270

8

Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenylalaninemia in southern Europe.

Guldberg P, Romano V, Ceratto N, Bosco P, Ciuna M, Indelicato A, Mollica F, Meli C, Giovannini M, Riva E, et al. Guldberg P, et al. Among authors: ceratto n. Hum Mol Genet. 1993 Oct;2(10):1703-7. doi: 10.1093/hmg/2.10.1703. Hum Mol Genet. 1993. PMID: 8268925

9

Association between haplotypes, hind III-VNTR alleles and mutations at the PAH locus in Sicily.

Romano V, Calì F, Guldberg P, Güttler F, Indelicato A, Bosco P, Ceratto N. Romano V, et al. Among authors: ceratto n. Acta Paediatr Suppl. 1994 Dec;407:39-40. doi: 10.1111/j.1651-2227.1994.tb13446.x. Acta Paediatr Suppl. 1994. PMID: 7766953

10

Chromosomal mapping of human cytokeratin 13 gene (KRT13).

Romano V, Raimondi E, Bosco P, Feo S, Di Pietro C, Leube RE, Troyanovsky SM, Ceratto N. Romano V, et al. Among authors: ceratto n. Genomics. 1992 Oct;14(2):495-7. doi: 10.1016/s0888-7543(05)80250-2. Genomics. 1992. PMID: 1385306

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