Carella M - Search Results

1

A YAC contig spanning the blepharophimosis-ptosis-epicanthus inversus syndrome and propionic acidemia loci.

Piemontese MR, Memeo E, Carella M, Amati P, Chomel JC, Bonneau D, Pilia G, Cao A, Drabkin H, Gemmill R, Rommens J, Zelante L, Gasparini P, Bisceglia L. Piemontese MR, et al. Among authors: carella m. Eur J Hum Genet. 1997 May-Jun;5(3):171-4. Eur J Hum Genet. 1997. PMID: 9272742

2

Hereditary hemochromatosis: generation of a transcription map within a refined and extended map of the HLA class I region.

Totaro A, Rommens JM, Grifa A, Lunardi C, Carella M, Huizenga JJ, Roetto A, Camaschella C, De Sandre G, Gasparini P. Totaro A, et al. Among authors: carella m. Genomics. 1996 Feb 1;31(3):319-26. doi: 10.1006/geno.1996.0054. Genomics. 1996. PMID: 8838313

3

Construction of a YAC contig covering human chromosome 6p22.

Malaspina P, Roetto A, Trettel F, Jodice C, Blasi P, Frontali M, Carella M, Franco B, Camaschella C, Novelletto A. Malaspina P, et al. Among authors: carella m. Genomics. 1996 Sep 15;36(3):399-407. doi: 10.1006/geno.1996.0484. Genomics. 1996. PMID: 8884262 Free article.

4

Two polymorphic repeats in the candidate region for the haemochromatosis gene.

Grifa A, Totaro A, Carella M, D'Ambrosio L, Sbaiz L, Roetto A, Camaschella C, Gasparini P. Grifa A, et al. Among authors: carella m. Mol Cell Probes. 1996 Dec;10(6):469-70. doi: 10.1006/mcpr.1996.0065. Mol Cell Probes. 1996. PMID: 9025086 No abstract available.

5

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients.

Carella M, D'Ambrosio L, Totaro A, Grifa A, Valentino MA, Piperno A, Girelli D, Roetto A, Franco B, Gasparini P, Camaschella C. Carella M, et al. Am J Hum Genet. 1997 Apr;60(4):828-32. Am J Hum Genet. 1997. PMID: 9106528 Free PMC article.

6

Hereditary hemochromatosis: a HpaI polymorphism within the HLA-H gene.

Totaro A, Grifa A, Carella M, D'Ambrosio L, Valentino M, Roth MP, Borot N, Coppin H, Roetto A, Camaschella C, Gasparini P. Totaro A, et al. Among authors: carella m. Mol Cell Probes. 1997 Jun;11(3):229-30. doi: 10.1006/mcpr.1997.0102. Mol Cell Probes. 1997. PMID: 9232622 No abstract available.

7

A frequent polymorphism in the 5' region of the BCMA gene.

Roetto A, Cicilano M, Gottardi E, Totaro A, Carella M, Gasparini P, Camaschella C. Roetto A, et al. Among authors: carella m. Mol Cell Probes. 1997 Aug;11(4):311-2. doi: 10.1006/mcpr.1997.0115. Mol Cell Probes. 1997. PMID: 9281419 No abstract available.

8

A recombination event close to HFE gene in hereditary hemochromatosis.

Roetto A, Sbaiz L, Bosio S, Piperno A, Fargion S, Carella M, Totaro A, Grifa A, Gasparini P, Camaschella C. Roetto A, et al. Among authors: carella m. Ann Genet. 1997;40(3):150-3. Ann Genet. 1997. PMID: 9401103 Free article.

9

Juvenile and adult hemochromatosis are distinct genetic disorders.

Camaschella C, Roetto A, Cicilano M, Pasquero P, Bosio S, Gubetta L, Di Vito F, Girelli D, Totaro A, Carella M, Grifa A, Gasparini P. Camaschella C, et al. Among authors: carella m. Eur J Hum Genet. 1997 Nov-Dec;5(6):371-5. Eur J Hum Genet. 1997. PMID: 9450181

10

Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).

Carella M, Stewart G, Ajetunmobi JF, Perrotta S, Grootenboer S, Tchernia G, Delaunay J, Totaro A, Zelante L, Gasparini P, Iolascon A. Carella M, et al. Am J Hum Genet. 1998 Sep;63(3):810-6. doi: 10.1086/302024. Am J Hum Genet. 1998. PMID: 9718354 Free PMC article.

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