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Morris, Michael Andréw

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2013

Scientific Articles

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First evidence of a polygenic susceptibility to pain in a pediatric cohort

Mamie, Chantal; Rebsamen, Michela; Morris, Michael Andréw; Morabia, Alfredo;

2012

Scientific Articles

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Intranasal calcitonin reducing bone pain in a patient with Camurati-Engelmann disease

Trombetti, Andrea; Cortes, Flavio; Kaelin, André; Morris, Michael Andréw; Rizzoli, René

2011

Scientific Articles

unige:32205	Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report	Hamamy, Hanan; Antonarakis, Stylianos; Cavalli-Sforza, Luigi Luca; Temtamy, Samia; ... Bittles, Alan H
unige:25377	Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing	Ratnamala, Uppala; Lyle, Robert; Rawal, Rakesh; Singh, Raminder; ... Radhakrishna, Uppala

2010

Scientific Articles

unige:21080	A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation	Le Gal, Francois; Korff, Christian; Monso-Hinard, Christine; Mund, Michael T.; ... Schmitt-Mechelke, Thomas
unige:21377	Alpha-1-antitrypsin deficiency in a 78-year-old woman with isolated liver cirrhosis	Voide, Nathalie; Ardigo, Sheila; Morris, Michael Andréw; Rubbia-Brandt, Laura; ... Vischer, Ulrich Max
unige:21106	De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic features	Makrythanasis, Periklis; Moix, Isabelle; Gimelli, Stefania; Fluss, Joel Victor; ... Bottani, Armand

2008

Scientific Articles

unige:1923	Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype-genotype correlation	Djambas Khayat, C.; Salem, N.; Chouery, E.; Corbani, S.; ... Mégarbané, A.
unige:1188	Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events	Dahoun, Sophie; Gagos, Sarantis; Gagnebin, Maryline; Gehrig, Corinne; ... Blouin, Jean-Louis
unige:8884	Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients	Martinet, Danielle; Filges, Isabel; Besuchet Schmutz, Nathalie; Morris, Michael Andréw; ... Bena, Frédérique

2007

Scientific Articles

unige:8764	Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome	Gothelf, Doron; Hoeft, Fumiko; Hinard, Christine; Hallmayer, J. F.; ... Reiss, A. L.
unige:45494	Expanding the phenotype of fragile X-associated tremor/ataxia syndrome: a new female case	Horvath, Judit; Burkhard, Pierre; Morris, Michael Andréw; Bottani, Armand; ... Delavelle, Jacqueline
unige:8702	MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother	Dayer, Alexandre; Bottani, Armand; Bouchardy, Isabelle; Fluss, Joel Victor; ... Morris, Michael Andréw

2006

Scientific Articles

unige:8741	Combined factor V - factor VIII deficiency (F5F8D): compound heterozygosity for two novel truncating mutations in LMAN1 in a consanguineous patient	Farah, R. A.; De Moerloose, Philippe; Bouchardy, Isabelle; Morris, Michael Andréw; ... Neerman Arbez, Marguerite
unige:5369	No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome	Glaser, Bronwyn; Debbané, Martin; Hinard, Christine; Morris, Michael Andréw; ... Eliez, Stéphan

2005

Scientific Articles

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COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

Gothelf, Doron; Eliez, Stéphan; Thompson, Tracy; Hinard, Christine; ... Reiss, A. L.

2004

Scientific Articles

unige:8932	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, Marguerite; Germanos-Haddad, Myrna; Tzanidakis, Konstantinos; Vu, Dung; ... De Moerloose, Philippe
unige:7208	The role of CFTR and SPINK-1 mutations in pancreatic disorders in HIV-positive patients: a case-control study	Felley, Christian; Morris, Michael Andréw; Wonkam, Ambroise; Hirschel, Bernard; ... Frossard, Jean-Louis

2003

Scientific Articles

unige:9079	Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion	Vu, Dung; Bolton-Maggs, P. H.; Parr, J. R.; Morris, Michael Andréw; ... Neerman Arbez, Marguerite
unige:9097	DNA deamination enables direct PCR amplification of the cystatin B (CSTB) gene-associated dodecamer repeat expansion in myoclonus epilepsy type Unverricht-Lundborg	Weinhaeusel, Andreas; Morris, Michael Andréw; Antonarakis, Stylianos; Haas, O. A.;
unige:8937	Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family	Neerman Arbez, Marguerite; Vu, Dung; Abu-Libdeh, Bassam; Bouchardy, Isabelle; Morris, Michael Andréw

2002

Scientific Articles

unige:9037	A t(2;8) balanced translocation with breakpoints near the human HOXD complex causes mesomelic dysplasia and vertebral defects	Spitz, François; Montavon, Thomas; Monso-Hinard, Christine; Morris, Michael Andréw; ... Duboule, Denis
unige:8758	Language skills in children with velocardiofacial syndrome (deletion 22q11.2)	Glaser, Bronwyn; Mumme, D. L.; Blasey, Christine; Morris, Michael Andréw; ... Eliez, Stéphan

2001

Scientific Articles

unige:8619	Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G→T	Attanasio, Catia; De Moerloose, Philippe; Antonarakis, Stylianos; Morris, Michael Andréw; Neerman Arbez, Marguerite
unige:8931	Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes	Neerman Arbez, Marguerite; De Moerloose, Philippe; Honsberger, A.; Parlier, G.; ... Morris, Michael Andréw
unige:8734	Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary study	Eliez, Stéphan; Antonarakis, Stylianos; Morris, Michael Andréw; Dahoun, S. P.; Reiss, A. L.

2000

Scientific Articles

unige:27051	Cystic fibrosis transmembrane conductance regulator does not affect neutrophil migration across cystic fibrosis airway epithelial monolayers	Pizurki, Lara Johanna; Morris, Michael Andréw; Chanson, Marc; Solomon, Melete; ... Suter, Susanne
unige:8930	Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia	Neerman Arbez, Marguerite; De Moerloose, Philippe; Bridel, C.; Honsberger, A.; ... Morris, Michael Andréw

1999

Scientific Articles

unige:8681	A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y	Chen, H.; Rossier, Colette; Morris, Michael Andréw; Scott, Hamish Steele; ... Antonarakis, Stylianos
unige:8624	Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping	Bartoloni, Lucia; Blouin, Jean-Louis; Sainsbury, A. J.; Gos, A.; ... Antonarakis, Stylianos
unige:8934	Deletion of the fibrogen alpha-chain gene (FGA) causes congenital afibrogenemia	Neerman Arbez, Marguerite; Honsberger, A.; Antonarakis, Stylianos; Morris, Michael Andréw;
unige:8905	Isolation and characterization of the mouse Aire gene	Mittaz, L.; Rossier, Colette; Heino, M.; Peterson, P.; ... Scott, Hamish Steele
unige:8935	Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency	Neerman Arbez, Marguerite; Johnson, K. M.; Morris, Michael Andréw; McVey, J. H.; ... Tuddenham, E. G.
unige:8927	The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster	Neerman Arbez, Marguerite; Antonarakis, Stylianos; Honsberger, A.; Morris, Michael Andréw;

1998

Scientific Articles

unige:9148	Gene structure and chromosomal localization of the human P2X7 receptor	Buell, G. N.; Talabot, F.; Gos, A.; Lorenz, J.; ... Antonarakis, Stylianos
unige:10349	Needle muscle biopsy in the investigation of neuromuscular disorders	Magistris, M. R.; Kohler, André; Pizzolato, G.; Morris, Michael Andréw; ... Bader, Charles

1997

Scientific Articles

unige:8628	A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region	Bartsch, O.; Hinkel, G. K.; Petersen, M. B.; Konig, U.; ... Antonarakis, Stylianos
unige:9076	Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency	Villard, Jean; Reith, Walter; Barras, Emmanuele; Gos, A.; ... Mach, Bernard
unige:8847	Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy	Lalioti, M. D.; Scott, Hamish Steele; Buresi, C.; Rossier, Colette; ... Antonarakis, Stylianos
unige:8735	Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13	Eliez, Stéphan; Morris, Michael Andréw; Dahoun-Hadorn, S.; DeLozier-Blanchet, C. D.; ... Antonarakis, Stylianos
unige:8642	Fortuitous detection of uniparental isodisomy of chromosome 6	Bittencourt, M. C.; Morris, Michael Andréw; Chabod, J.; Gos, A.; ... Tiberghien, P.

1996

Scientific Articles

unige:8676	Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping	Chen, H.; Chrast, R.; Rossier, Colette; Morris, Michael Andréw; ... Antonarakis, Stylianos
unige:8677	Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter	Chen, H.; Gos, A.; Morris, Michael Andréw; Antonarakis, Stylianos;
unige:8648	Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21	Blouin, Jean-Louis; Duriaux Sail, Geneviève; Chen, H.; Gos, A.; ... Antonarakis, Stylianos
unige:8843	The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3	Lalioti, M. D.; Gos, A.; Green, M. R.; Rossier, Colette; ... Antonarakis, Stylianos
unige:8963	Two novel mutations affecting mRNA splicing of the neurofibromatosis type 1 (NF1) gene	Perrin, G.; Morris, Michael Andréw; Antonarakis, Stylianos; Boltshauser, E.; Hutter, Pierre

1995

Scientific Articles

unige:8645	A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination	Blouin, Jean-Louis; Christie, D. H.; Gos, A.; Lynn, A.; ... Antonarakis, Stylianos
unige:9264	Characterization and chromosomal localization of a human P2X receptor from the urinary bladder	Valera, S.; Talabot, F.; Evans, R. J.; Gos, A.; ... Buell, G. N.
unige:8678	Cloning of the cDNA for the human ATP synthase OSCP subunit (ATP5O) by exon trapping and mapping to chromosome 21q22.1-q22.2	Chen, H.; Morris, Michael Andréw; Rossier, Colette; Blouin, Jean-Louis; Antonarakis, Stylianos
unige:54889	Ischaemic colitis due to mitochondrial cytopathy	Hess, J; Burkhard, Pierre; Morris, Michael Andréw; Lalioti, M; ... Hadengue, Antoine

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