Found: 7
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Understanding the impact of 1q21.1 copy number variant.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Aggressive B‐cell lymphoma with t(3;8)(q27;q24) in an elderly patient.
- Published in:
- American Journal of Hematology, 2022, v. 97, n. 7, p. 986, doi. 10.1002/ajh.26430
- By:
- Publication type:
- Article
Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders.
- Published in:
- Journal of Autism & Developmental Disorders, 2012, v. 42, n. 7, p. 1459, doi. 10.1007/s10803-011-1389-4
- By:
- Publication type:
- Article
Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 4, p. 458, doi. 10.1038/ejhg.2013.185
- By:
- Publication type:
- Article
Chronic Lymphocytic Leukemia Patients With Deletion 11q Have a Short Time to Requirement of First-Line Therapy, But Long Overall Survival: Results of a Population-Based Cohort in British Columbia, Canada.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Influence of Clone and Deletion Size on Outcome in Chronic Lymphocytic Leukemia Patients with an Isolated Deletion 13q in a Population-Based Analysis in British Columbia, Canada.
- Published in:
- Genes, Chromosomes & Cancer, 2016, v. 55, n. 1, p. 16, doi. 10.1002/gcc.22294
- By:
- Publication type:
- Article
Prenatal cytogenetic assessment and inv(2)(p11.2q13).
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 9, p. 810, doi. 10.1002/pd.1508
- By:
- Publication type:
- Article