Morris MA - Search Results

1

Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes.

Neerman-Arbez M, de Moerloose P, Honsberger A, Parlier G, Arnuti B, Biron C, Borg JY, Eber S, Meili E, Peter-Salonen K, Ripoll L, Vervel C, d'Oiron R, Staeger P, Antonarakis SE, Morris MA. Neerman-Arbez M, et al. Among authors: morris ma. Hum Genet. 2001 Mar;108(3):237-40. doi: 10.1007/s004390100469. Hum Genet. 2001. PMID: 11354637

2

Deletion of the fibrinogen [correction of fibrogen] alpha-chain gene (FGA) causes congenital afibrogenemia.

Neerman-Arbez M, Honsberger A, Antonarakis SE, Morris MA. Neerman-Arbez M, et al. Among authors: morris ma. J Clin Invest. 1999 Jan;103(2):215-8. doi: 10.1172/JCI5471. J Clin Invest. 1999. PMID: 9916133 Free PMC article.

3

The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster.

Neerman-Arbez M, Antonarakis SE, Honsberger A, Morris MA. Neerman-Arbez M, et al. Among authors: morris ma. Eur J Hum Genet. 1999 Dec;7(8):897-902. doi: 10.1038/sj.ejhg.5200395. Eur J Hum Genet. 1999. PMID: 10602365

4

Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia.

Neerman-Arbez M, de Moerloose P, Bridel C, Honsberger A, Schönbörner A, Rossier C, Peerlinck K, Claeyssens S, Di Michele D, d'Oiron R, Dreyfus M, Laubriat-Bianchin M, Dieval J, Antonarakis SE, Morris MA. Neerman-Arbez M, et al. Among authors: morris ma. Blood. 2000 Jul 1;96(1):149-52. Blood. 2000. PMID: 10891444 Free article.

5

Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G-->T.

Attanasio C, de Moerloose P, Antonarakis SE, Morris MA, Neerman-Arbez M. Attanasio C, et al. Among authors: morris ma. Blood. 2001 Mar 15;97(6):1879-81. doi: 10.1182/blood.v97.6.1879. Blood. 2001. PMID: 11238133 Free article.

6

Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.

Neerman-Arbez M, Vu D, Abu-Libdeh B, Bouchardy I, Morris MA. Neerman-Arbez M, et al. Among authors: morris ma. Blood. 2003 May 1;101(9):3492-4. doi: 10.1182/blood-2002-10-3116. Epub 2003 Jan 2. Blood. 2003. PMID: 12511408 Free article.

7

Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.

Vu D, Bolton-Maggs PH, Parr JR, Morris MA, de Moerloose P, Neerman-Arbez M. Vu D, et al. Among authors: morris ma. Blood. 2003 Dec 15;102(13):4413-5. doi: 10.1182/blood-2003-06-2141. Epub 2003 Jul 31. Blood. 2003. PMID: 12893758 Free article.

8

Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells.

Neerman-Arbez M, Germanos-Haddad M, Tzanidakis K, Vu D, Deutsch S, David A, Morris MA, de Moerloose P. Neerman-Arbez M, et al. Among authors: morris ma. Blood. 2004 Dec 1;104(12):3618-23. doi: 10.1182/blood-2004-06-2312. Epub 2004 Jul 29. Blood. 2004. PMID: 15284111 Free article.

9

Exon skipping associated with A-->G transition at +4 of the IVS33 splice donor site of the neurofibromatosis type 1 (NF1) gene.

Hutter P, Antonarakis SE, Delozier-Blanchet CD, Morris MA. Hutter P, et al. Among authors: morris ma. Hum Mol Genet. 1994 Apr;3(4):663-5. doi: 10.1093/hmg/3.4.663. Hum Mol Genet. 1994. PMID: 8069315 No abstract available.

10

Dinucleotide repeat polymorphism within ERCC5 gene.

Samec S, Clarkson SG, Blaschak J, Chakravarti A, Morris MA, Scherly D, Antonarakis SE. Samec S, et al. Among authors: morris ma. Hum Mol Genet. 1994 Jan;3(1):214. doi: 10.1093/hmg/3.1.214-a. Hum Mol Genet. 1994. PMID: 8162040 No abstract available.

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