Morris MA - Search Results

1

MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother.

Dayer AG, Bottani A, Bouchardy I, Fluss J, Antonarakis SE, Haenggeli CA, Morris MA. Dayer AG, et al. Among authors: morris ma. Brain Dev. 2007 Jan;29(1):47-50. doi: 10.1016/j.braindev.2006.06.001. Epub 2006 Jul 17. Brain Dev. 2007. PMID: 16844334

2

De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic features.

Makrythanasis P, Moix I, Gimelli S, Fluss J, Aliferis K, Antonarakis SE, Morris MA, Béna F, Bottani A. Makrythanasis P, et al. Among authors: morris ma. Clin Genet. 2010 Aug;78(2):175-80. doi: 10.1111/j.1399-0004.2010.01371.x. Epub 2010 Jan 5. Clin Genet. 2010. PMID: 20236124

3

No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome.

Glaser B, Debbane M, Hinard C, Morris MA, Dahoun SP, Antonarakis SE, Eliez S. Glaser B, et al. Among authors: morris ma. Am J Psychiatry. 2006 Mar;163(3):537-9. doi: 10.1176/appi.ajp.163.3.537. Am J Psychiatry. 2006. PMID: 16513880

4

Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients.

Martinet D, Filges I, Besuchet Schmutz N, Morris MA, Gaide AC, Dahoun S, Bottani A, Addor MC, Antonarakis SE, Beckmann JS, Béna F. Martinet D, et al. Among authors: morris ma. Am J Med Genet A. 2008 Aug 15;146A(16):2094-102. doi: 10.1002/ajmg.a.32414. Am J Med Genet A. 2008. PMID: 18629875

5

Homozygous deletion of a gene-free region of 4p15 in a child with multiple anomalies: could biallelic loss of conserved, non-coding elements lead to a phenotype?

Makrythanasis P, Gimelli S, Béna F, Dahoun S, Morris MA, Antonarakis SE, Bottani A. Makrythanasis P, et al. Among authors: morris ma. Eur J Med Genet. 2012 Jan;55(1):63-6. doi: 10.1016/j.ejmg.2011.11.001. Epub 2011 Nov 10. Eur J Med Genet. 2012. PMID: 22080113

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

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.

8

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.

9

Molecular etiology of factor VIII deficiency in hemophilia A.

Antonarakis SE, Kazazian HH, Gitschier J, Hutter P, de Moerloose P, Morris MA. Antonarakis SE, et al. Among authors: morris ma. Adv Exp Med Biol. 1995;386:19-34. doi: 10.1007/978-1-4613-0331-2_2. Adv Exp Med Biol. 1995. PMID: 8851012 Review. No abstract available.

10

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

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