Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome
Mazzeu, JF, Vianna-Morgante, AM, Krepischi, ACV, Oudakker, A, Rosenberg, C, Szuhai, K, McGill, J, MacCraughan, J, Van Bokhoven, H, Brunner, HG
Published in Clinical genetics (01.04.2010)
Published in Clinical genetics (01.04.2010)
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Chromosome imbalances in syndromic hearing loss
Catelani, ALPM, Krepischi, ACV, Kim, CA, Kok, F, Otto, PA, Auricchio, MTBM, Mazzeu, JF, Uehara, DT, Costa, SS, Knijnenburg, J, Tabith Jr, A, Vianna-Morgante, AM, Mingroni-Netto, RC, Rosenberg, C
Published in Clinical genetics (01.11.2009)
Published in Clinical genetics (01.11.2009)
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Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents
Rosenberg, C, Knijnenburg, J, Bakker, E, Vianna-Morgante, A M, Sloos, W, Otto, P A, Kriek, M, Hansson, K, Krepischi-Santos, A C V, Fiegler, H, Carter, N P, Bijlsma, E K, van Haeringen, A, Szuhai, K, Tanke, H J
Published in Journal of medical genetics (01.02.2006)
Published in Journal of medical genetics (01.02.2006)
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Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases
Carneiro, Thaise Nr, Krepischi, Ana Cv, Costa, Silvia S, Tojal da Silva, Israel, Vianna-Morgante, Angela M, Valieris, Renan, Ezquina, Suzana Am, Bertola, Debora R, Otto, Paulo A, Rosenberg, Carla
Published in Application of clinical genetics (01.01.2018)
Published in Application of clinical genetics (01.01.2018)
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Crotamine is a novel cell-penetrating protein from the venom of rattlesnake Crotalus durissus terrificus
Kerkis, Alexandre, Kerkis, Irina, Rádis-Baptista, Gandhi, Oliveira, Eduardo B, Vianna-Morgante, Angela M, Pereira, Lygia V, Yamane, Tetsuo
Published in The FASEB journal (01.09.2004)
Published in The FASEB journal (01.09.2004)
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Molecular and clinical delineation of the 17q22 microdeletion phenotype
Laurell, Tobias, Lundin, Johanna, Anderlid, Britt-Marie, Gorski, Jerome L, Grigelioniene, Giedre, Knight, Samantha J L, Krepischi, Ana C V, Nordenskjöld, Agneta, Price, Susan M, Rosenberg, Carla, Turnpenny, Peter D, Vianna-Morgante, Angela M, Nordgren, Ann
Published in European journal of human genetics : EJHG (01.10.2013)
Published in European journal of human genetics : EJHG (01.10.2013)
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An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array‐CGH) defines a new locus (FGS5) for FG syndrome
Jehee, Fernanda Sarquis, Rosenberg, Carla, Krepischi‐Santos, Ana Cristina, Kok, Fernando, Knijnenburg, Jeroen, Froyen, Guy, Vianna‐Morgante, Angela M., Opitz, John M., Passos‐Bueno, Maria Rita
Published in American journal of medical genetics. Part A (15.12.2005)
Published in American journal of medical genetics. Part A (15.12.2005)
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Journal Article
Structure and chromosomal localization of the gene for crotamine, a toxin from the South American rattlesnake, Crotalus durissus terrificus
Rádis-Baptista, Gandhi, Kubo, Tai, Oguiura, Nancy, Svartman, Marta, Almeida, Therezinha M.B, Batistic, Radenka F, Oliveira, Eduardo B, Vianna-Morgante, Ângela M, Yamane, Tetsuo
Published in Toxicon (Oxford) (01.12.2003)
Published in Toxicon (Oxford) (01.12.2003)
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Does the P172H mutation at the TM4SF2 gene cause X-linked mental retardation?
Maranduba, Carlos Magno da Costa, Sá Moreira, Eloísa, Müller Orabona, Guilherme, Cássia Pavanello, Rita, Vianna-Morgante, Angela M., Rita Passos-Bueno, Maria
Published in American journal of medical genetics. Part A (01.02.2004)
Published in American journal of medical genetics. Part A (01.02.2004)
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Journal Article
AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations
Angeli, Claudia B., Capelli, Leonardo P., Auricchio, Maria Teresa B.M., Vianna-Morgante, Angela M., Mingroni-Netto, Regina C., Leal-Mesquita, Emygdia R., Ribeiro-dos-Santos, Ândrea K.C., Ferrari, Iris, Oliveira, Silviene F., Klautau-Guimarães, Maria de Nazaré
Published in American journal of medical genetics. Part A (01.07.2005)
Published in American journal of medical genetics. Part A (01.07.2005)
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Structure and stability upon maternal transmission of common and intermediate FMR1 (Fragile X Mental Retardation 1) alleles in a sample of the Brazilian population
Capelli, Leonardo P., Mingroni-Netto, Regina C., Vianna-Morgante, Angela M.
Published in Genetics and molecular biology (01.03.2005)
Published in Genetics and molecular biology (01.03.2005)
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Journal Article
AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations
Angeli, Claudia B., Capelli, Leonardo P., Auricchio, Maria Teresa B.M., Vianna-Morgante, Angela M., Mingroni-Netto, Regina C., Leal-Mesquita, Emygdia R., Ribeiro-dos-Santos, Ândrea K.C., Ferrari, Iris, Oliveira, Silviene F., Klautau-Guimarães, Maria de Nazaré
Published in American journal of medical genetics. Part A (15.01.2005)
Published in American journal of medical genetics. Part A (15.01.2005)
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