A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation
P. J. Hastings, Grzegorz Ira, James R. Lupski · PLoS Genetics · 2009 · Review
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Genetic Etiologies for Phenotypic Diversity in Sickle Cell Anemia
Martin H. Steinberg · The Scientific World JOURNAL · 2009 · Review
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Concerns about anti-angiogenic treatment in patients with glioblastoma multiforme
Joost JC Verhoeff, Olaf van Tellingen, An Claes et al. · BMC Cancer · 2009 · Review
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Pervasive Natural Selection in the Drosophila Genome?
Guy Sella, Dmitri A. Petrov, Molly Przeworski et al. · PLoS Genetics · 2009 · Review
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Role of paracrine factors in stem and progenitor cell mediated cardiac repair and tissue fibrosis
Jana S Burchfield, Stefanie Dimmeler · Fibrogenesis & Tissue Repair · 2008 · Review
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Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference
Adrianna Vlachos, Sarah Ball, Niklas Dahl et al. · British Journal of Haematology · 2008 · Review
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Sickle Cell Anemia, the First Molecular Disease: Overview of Molecular Etiology, Pathophysiology, and Therapeutic Approaches
Martin H. Steinberg · The Scientific World JOURNAL · 2008 · Review
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Ehlers-Danlos syndrome type IV
Dominique P Germain · Orphanet Journal of Rare Diseases · 2007 · Review
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Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
Xavier Estivill, Lluís Armengol · PLoS Genetics · 2007 · Review
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Klinefelter syndrome and other sex chromosomal aneuploidies
Jeannie Visootsak, John M Graham · Orphanet Journal of Rare Diseases · 2006 · Review
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Cri du Chat syndrome
Paola Cerruti Mainardi · Orphanet Journal of Rare Diseases · 2006 · Review
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