Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Report
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A 10.46 Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autismSoysal, Yasemin ; Vermeesch, Joris ; Davani, Nooshin Ardeshir ; Hekimler, Kuyaş ; İmirzalıoğlu, NecatAmerican Journal of Medical Genetics Part A, 2011, Vol.155A (7), p.1745-1752Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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2 |
Material Type: Report
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A case of autism with an interstitial 1q deletion (1q23.3-24.2) and a de novo translocation of chromosomes 1q and 5qDella Monica, Matteo ; Lonardo, Fortunato ; Faravelli, Francesca ; Pierluigi, Mauro ; Luquetti, Daniela Varela ; De Gregori, Manuela ; Zuffardi, Orsetta ; Scarano, GioacchinoAmerican Journal of Medical Genetics Part A, 2007, Vol.143A (22), p.2733-2737Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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3 |
Material Type: Report
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Cervical tumoral calcinosis with secondary hyperparathyroidism in a chronic hemodialysis patientSunder, Sham ; Verma, Himanshu ; Venkataramanan, KrishnamoorthyHemodialysis International, 2013, Vol.17 (3), p.458-462Blackwell Publishing LtdTexto completo disponível |
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4 |
Material Type: Report
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Compensatory education for cultural deprivation, B. S. Bloom, A. Davis, R. Hess. 1965Segré, MoniqueRevue française de pédagogie, 1967, Vol.1 (1), p.39-40PERSÉE : Université de Lyon, CNRS & ENS de LyonTexto completo disponível |
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5 |
Material Type: Report
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Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sistersHarrison, Victoria ; Connell, Lyndsey ; Hayesmoore, Jesse ; McParland, Joanna ; Pike, Michael G. ; Blair, EdwardAmerican Journal of Medical Genetics Part A, 2011, Vol.155A (11), p.2826-2831Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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6 |
Material Type: Report
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Deep pyoderma caused by Burkholderia cepacia complex associated with ciclosporin administration in dogs: a case seriesBanovic, Frane ; Koch, Sandra ; Robson, David ; Jacob, Megan ; Olivry, ThierryVeterinary Dermatology, 2015, Vol.26 (4), p.287-e64Blackwell Publishing LtdTexto completo disponível |
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7 |
Material Type: Report
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Fanconi's Syndrome in a Dog With Primary HypoparathyroidismFreeman, Lisa M. ; Breitschwerdt, Edward B. ; Keene, Bruce W. ; Hansen, BernieJournal of Veterinary Internal Medicine, 1994, Vol.8 (5), p.349-354Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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8 |
Material Type: Report
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High Energy Alpha Particles Associated with FissionWollan, E. O ; Moak, Charles D ; Sawyer, R. B1947Texto completo disponível |
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9 |
Material Type: Report
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Mosaic partial trisomy 19p12-q13.11 due to a small supernumerary marker chromosome: A locus associated with Asperger syndrome?Faucz, Fabio Rueda ; Souza, Josiane ; Filho, Aguinaldo Bonalumi ; Sotomaior, Vanessa Santos ; Frantz, Egon ; Antoniuk, Sergio ; Rosenfeld, Jill A. ; Raskin, SalmoAmerican Journal of Medical Genetics Part A, 2011, Vol.155A (9), p.2308-2310Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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10 |
Material Type: Report
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Resolution of coronary arteritis following tuberculosis treatmentBarreto-Neto, Nestor ; Segre, Alexandre W ; Guedes, Lissiane K N ; Seguro, Luciana P C ; Pereira, Rosa M RJournal of clinical tuberculosis and other mycobacterial diseases, 2022, Vol.26, p.100295-100295Texto completo disponível |