Found: 16
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Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomes.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-34053-7
- By:
- Publication type:
- Article
A Novel de novo FZD2 Mutation in a Patient with Autosomal Dominant Omodysplasia.
- Published in:
- Molecular Syndromology, 2017, v. 8, n. 6, p. 318, doi. 10.1159/000479721
- By:
- Publication type:
- Article
Aneuploidy in children with relapsed B‐cell precursor acute lymphoblastic leukaemia: clinical importance of detecting a hypodiploid origin of relapse.
- Published in:
- British Journal of Haematology, 2019, v. 185, n. 2, p. 266, doi. 10.1111/bjh.15770
- By:
- Publication type:
- Article
The time of onset of abnormal calcification in spondylometaepiphyseal dysplasia, short limb-abnormal calcification type.
- Published in:
- Pediatric Radiology, 2009, v. 39, n. 1, p. 84, doi. 10.1007/s00247-008-1036-1
- By:
- Publication type:
- Article
Flow cytometric maturity score as a novel prognostic parameter in patients with acute myeloid leukemia.
- Published in:
- Annals of Hematology, 2015, v. 94, n. 8, p. 1337, doi. 10.1007/s00277-015-2400-5
- By:
- Publication type:
- Article
Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 11, p. 858, doi. 10.1038/sj.ejhg.5201050
- By:
- Publication type:
- Article
Synergistic action of the novel HSP90 inhibitor NVP-AUY922 with histone deacetylase inhibitors, melphalan, or doxorubicin in multiple myeloma.
- Published in:
- European Journal of Haematology, 2010, v. 84, n. 4, p. 337, doi. 10.1111/j.1600-0609.2009.01403.x
- By:
- Publication type:
- Article
A Rare Case of Acute Myeloid Leukemia with a t(2;3) Chromosomal Translocation Characterized by Thrombophilia and Chemoresistance.
- Published in:
- Journal of Clinical & Experimental Hematopathology, 2016, v. 56, n. 1, p. 64, doi. 10.3960/jslrt.56.64
- By:
- Publication type:
- Article
High prevalence of immunoglobulin light chain gene aberrations as revealed by FISH in multiple myeloma and MGUS.
- Published in:
- Genes, Chromosomes & Cancer, 2014, v. 53, n. 8, p. 650, doi. 10.1002/gcc.22175
- By:
- Publication type:
- Article
Involvement of the MLL gene in adult T-lymphoblastic leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2012, v. 51, n. 12, p. 1114, doi. 10.1002/gcc.21996
- By:
- Publication type:
- Article
A BACH2-BCL2L1 fusion gene resulting from a t(6;20)(q15;q11.2) chromosomal translocation in the lymphoma cell line BLUE-1.
- Published in:
- Genes, Chromosomes & Cancer, 2011, v. 50, n. 6, p. 389, doi. 10.1002/gcc.20863
- By:
- Publication type:
- Article
CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 5, p. 1
- By:
- Publication type:
- Article
Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 12, p. 2149, doi. 10.1093/hmg/ddp148
- By:
- Publication type:
- Article
BCR-ABL1 Acute Myeloid Leukemia: Clonal Selection of a BCR-ABL1<sup>-</sup> Subclone as a Cause of Refractory Disease with Nilotinib Treatment.
- Published in:
- Acta Haematologica, 2015, v. 133, n. 2, p. 237, doi. 10.1159/000368176
- By:
- Publication type:
- Article
TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies.
- Published in:
- Human Mutation, 2002, v. 20, n. 3, p. 197, doi. 10.1002/humu.10112
- By:
- Publication type:
- Article