Highlights
Morris, Michael Andréw
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2013
Scientific Articles
unige:35220![]() ![]() | First evidence of a polygenic susceptibility to pain in a pediatric cohort | Mamie, Chantal; Rebsamen, Michela; Morris, Michael Andréw; Morabia, Alfredo; |
2012
Scientific Articles
unige:31682![]() ![]() | 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 | Antonarakis, Stylianos; Fokstuen, Siv; Engel, Eric; Dermitzakis, Emmanouil; ... Mostafavi, Maryam |
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
2005
Scientific Articles
unige:8763![]() ![]() | 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
2003
Scientific Articles
2002
Scientific Articles
2001
Scientific Articles
2000
Scientific Articles
1999
Scientific Articles
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
1996
Scientific Articles
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 |