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Mapping of Deletional Forms of α- and γδβ-Thalassemia.
- Published in:
- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 480, doi. 10.1111/j.1749-6632.1990.tb24337.x
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- Article
Rheological Properties of SickleErythrocytes in the Steady State Predict the Frequency and Severity of the Sickle Cell Painful Crisis.
- Published in:
- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 363, doi. 10.1111/j.1749-6632.1989.tb24188.x
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- Article
The Effect of Alpha Thalassemia on the Clinical Course of Hemoglobin SC Disease.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 365, doi. 10.1111/j.1749-6632.1989.tb24189.x
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- Article
Donor splice-site mutation in CUL4B is likely cause of X-linked intellectual disability.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 9, p. 2294, doi. 10.1002/ajmg.a.36629
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- Article
Digital mRNA profiling.
- Published in:
- Nature Biotechnology, 2008, v. 26, n. 3, p. 293, doi. 10.1038/nbt0308-293
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- Article
High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 2, p. 178, doi. 10.1038/ejhg.2009.154
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- Article
Simple two-color array-based approach for mutation detection.
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- European Journal of Human Genetics, 2000, v. 8, n. 11, p. 884, doi. 10.1038/sj.ejhg.5200558
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- Article
Parallel molecular genetic analysis.
- Published in:
- European Journal of Human Genetics, 1998, v. 6, n. 5, p. 417, doi. 10.1038/sj.ejhg.5200218
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- Article
α THALASSEMIA AND THE EXPRESSION OF HEMOGLOBIN G-PHILADELPHIA *.
- Published in:
- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 62, doi. 10.1111/j.1749-6632.1980.tb33649.x
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- Article
Kinetics of heterogeneous hybridization on indium tin oxide surfaces with and without an applied potential.
- Published in:
- Electrophoresis, 2002, v. 23, n. 10, p. 1551, doi. 10.1002/1522-2683(200205)23:10<1551::AID-ELPS1551>3.0.CO;2-9
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- Publication type:
- Article
Human α-Thalassemia syndromes: Detection of molecular defects.
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- American Journal of Hematology, 1996, v. 53, n. 2, p. 81, doi. 10.1002/(SICI)1096-8652(199610)53:2<81::AID-AJH5>3.0.CO;2-#
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- Publication type:
- Article
Generation of patterns from gene expression data by assigning confidence to differentially expressed genes.
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- Bioinformatics, 2000, v. 16, n. 8, p. 685, doi. 10.1093/bioinformatics/16.8.685
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- Article
Reply to ‘Gender-specific disease modification by NOS3’.
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- 2004
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- Publication type:
- Letter
Identification of APC gene mutations in colorectal cancer using universal microarray-based combinatorial sequencing-by-hybridization.
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- Human Mutation, 2004, v. 24, n. 3, p. 261, doi. 10.1002/humu.20078
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- Article
Pyrosequencing for detection of mutations in the connexin 26 (GJB2) and mitochondrial 12S RNA (MTRNR1) genes associated with hereditary hearing loss.
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- Human Mutation, 2002, v. 20, n. 4, p. 312, doi. 10.1002/humu.10127
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- Publication type:
- Article
Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 9, p. 1605, doi. 10.1093/hmg/6.9.1605
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- Article