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Síndrome de microdeleção 2q32 em paciente da Amazônia ocidental; 2q32 microdeletion syndrome in a patient from the western Amazon
Síndrome de microdeleção 2q32 em paciente da Amazônia ocidental; 2q32 microdeletion syndrome in a patient from the western Amazon
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Síndrome de microdeleção 2q32 em paciente da Amazônia ocidental; 2q32 microdeletion syndrome in a patient from the western Amazon

Oliveira, Wilyan Dias Cosmo; Silva, Christian Rogers Gomes Da; Andrade, Christopher Harrison Salomão; Borges, Edilson Moreira; Sá, Gabriele Batista De; Rocha, Joshua Werner Bicalho Da

Medicina (Ribeirao Preto); Vol. 56 No. 2 (2023); e-194793

Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto 2023-08-15

Acesso online

2
A Scalable Computational Approach for Simulating Complexes of Multiple Chromosomes
A Scalable Computational Approach for Simulating Complexes of Multiple Chromosomes
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A Scalable Computational Approach for Simulating Complexes of Multiple Chromosomes

Oliveira Junior, Antonio B. ; Contessoto, Vinícius G. ; Mello, Matheus F. ; Onuchic, José N.

Journal of molecular biology, 2021-03, Vol.433 (6), p.166700-166700, Article 166700 [Periódico revisado por pares]

England: Elsevier Ltd

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3
Mapping of MYC breakpoints in 8q24 rearrangements involving non-immunoglobulin partners in B-cell lymphomas
Mapping of MYC breakpoints in 8q24 rearrangements involving non-immunoglobulin partners in B-cell lymphomas
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Mapping of MYC breakpoints in 8q24 rearrangements involving non-immunoglobulin partners in B-cell lymphomas

BERTRAND, P ; BASTARD, C ; MAINGONNAT, C ; JARDIN, F ; MAISONNEUVE, C ; COUREL, M.-N ; RUMINY, P ; PICQUENOT, J.-M ; TILLY, H

Leukemia, 2007-03, Vol.21 (3), p.515-523 [Periódico revisado por pares]

London: Nature Publishing

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4
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2
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Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2

Zarate, Yuri A. ; Bosanko, Katherine A. ; Thomas, Mary Ann ; Miller, David T. ; Cusmano‐Ozog, Kristina ; Martinez‐Monseny, Antonio ; Curry, Cynthia J. ; Graham, John M. ; Velsher, Lea ; Bekheirnia, Mir Reza ; Seidel, Veronica ; Dedousis, Demitrios ; Mitchell, Anna L. ; DiMarino, Amy M. ; Riess, Angelika ; Balasubramanian, Meena ; Fish, Jennifer L. ; Caffrey, Aisling R. ; Fleischer, Nicole ; Pierson, Tyler Mark ; Lacro, Ronald V.

Clinical genetics, 2021-04, Vol.99 (4), p.547-557 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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5
Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma
Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma
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Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma

Martino, Alessandro ; Campa, Daniele ; Jamroziak, Krzysztof ; Reis, Rui Manuel ; Sainz, Juan ; Buda, Gabriele ; García-Sanz, Ramón ; Lesueur, Fabienne ; Marques, Herlander ; Moreno, Victor ; Jurado, Manuel ; Ríos, Rafael ; Szemraj-Rogucka, Zofia ; Szemraj, Janusz ; Tjønneland, Anne ; Overvad, Kim ; Vangsted, Annette Juul ; Vogel, Ulla ; Mikala, Gabor ; Kádár, Katalin ; Szombath, Gergely ; Varkonyi, Judit ; Orciuolo, Enrico ; Dumontet, Charles ; Gemignani, Federica ; Rossi, Anna Maria ; Landi, Stefano ; Petrini, Mario ; Houlston, Richard S. ; Hemminki, Kari ; Canzian, Federico

British journal of haematology, 2012-09, Vol.158 (6), p.805-809 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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6
Human Malformation Syndromes of Defective GLI: Opposite Phenotypes of 2q14.2 (GLI2) and 7p14.2 (GLI3) Microdeletions and a GLIA/R Balance Model
Human Malformation Syndromes of Defective GLI: Opposite Phenotypes of 2q14.2 (GLI2) and 7p14.2 (GLI3) Microdeletions and a GLIA/R Balance Model
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Human Malformation Syndromes of Defective GLI: Opposite Phenotypes of 2q14.2 (GLI2) and 7p14.2 (GLI3) Microdeletions and a GLIA/R Balance Model

Niida, Yo ; Inoue, Mika ; Ozaki, Mamoru ; Takase, Etsuko

Cytogenetic and genome research, 2017-01, Vol.153 (2), p.56-65 [Periódico revisado por pares]

Basel, Switzerland

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7
Triple‐hit B‐cell lymphoma, unclassifiable, with features intermediate between diffuse large B‐cell lymphoma and Burkitt lymphoma associated with a novel complex karyotype including t(2;3)(q21;q27), t(8;14)(q24;q32) and t(14;18)(q32;q21)
Triple‐hit B‐cell lymphoma, unclassifiable, with features intermediate between diffuse large B‐cell lymphoma and Burkitt lymphoma associated with a novel complex karyotype including t(2;3)(q21;q27), t(8;14)(q24;q32) and t(14;18)(q32;q21)
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Triple‐hit B‐cell lymphoma, unclassifiable, with features intermediate between diffuse large B‐cell lymphoma and Burkitt lymphoma associated with a novel complex karyotype including t(2;3)(q21;q27), t(8;14)(q24;q32) and t(14;18)(q32;q21)

Nakayama, Shoko ; Yokote, Taiji ; Iwaki, Kazuki ; Takayama, Ayami ; Tsuji, Motomu ; Hanafusa, Toshiaki

British journal of haematology, 2013-03, Vol.160 (5), p.569-569 [Periódico revisado por pares]

Oxford: Blackwell

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8
ALK-positive lymphoma : A single disease with a broad spectrum of morphology
ALK-positive lymphoma : A single disease with a broad spectrum of morphology
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ALK-positive lymphoma : A single disease with a broad spectrum of morphology

BENHARROCH, D ; MEGUERIAN-BEDOYAN, Z ; MASON, D. Y ; DELSOL, G ; LAMANT, L ; AMIN, C ; BRUGIERES, L ; TERRIER-LACOMBE, M.-J ; HARALAMBIEVA, E ; PULFORD, K ; PILERI, S ; MORRIS, S. W

Blood, 1998-03, Vol.91 (6), p.2076-2084 [Periódico revisado por pares]

Washington, DC: The Americain Society of Hematology

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9
Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1
Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1
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Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1

Rajcan-Separovic, E ; Harvard, C ; Liu, X ; McGillivray, B ; Hall, J G ; Qiao, Y ; Hurlburt, J ; Hildebrand, J ; Mickelson, E C R ; Holden, J J A ; Lewis, M E S

Journal of medical genetics, 2007-04, Vol.44 (4), p.269-276 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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10
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
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The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure

Scerri, Thomas S ; Darki, Fahimeh ; Newbury, Dianne F ; Whitehouse, Andrew J O ; Peyrard-Janvid, Myriam ; Matsson, Hans ; Ang, Qi W ; Pennell, Craig E ; Ring, Susan ; Stein, John ; Morris, Andrew P ; Monaco, Anthony P ; Kere, Juha ; Talcott, Joel B ; Klingberg, Torkel ; Paracchini, Silvia Baron, Jean-Claude

PloS one, 2012-11, Vol.7 (11), p.e50321-e50321 [Periódico revisado por pares]

United States: Public Library of Science

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Deste Autor:

  1. Rocha, J
  2. Silva, C
  3. Oliveira, W
  4. Andrade, C
  5. Sá, G

Neste Assunto:

  1. Humans
  2. Science & Technology
  3. Life Sciences & Biomedicine
  4. Biological And Medical Sciences
  5. Translocation, Genetic

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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