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Publications by Guilherme L Yamamoto
Large Deletion in PIGL: A Common Mutational Mechanism in CHIME Syndrome?
Genetics and Molecular Biology
Genetics
Molecular Biology
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A Large PROP1 Gene Deletion in a Turkish Pedigree
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A Large Deletion in the CFTR Gene in CBAVD
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Hereditary Hemorrhagic Telangiectasia: Breakpoint Characterization of a Novel Large Deletion inACVRL1Suggests the Causing Mechanism
Molecular Syndromology
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Complement Activation in 22q11.2 Deletion Syndrome
Journal of Clinical Immunology
Allergy
Immunology
The Mutational Spectrum of Lynch Syndrome in Cyprus
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Cryptic 5q Deletion in a Patient With Myelodysplastic Syndrome
British Journal of Haematology
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Acute Dystonia in a Patient With 22q11.2 Deletion Syndrome
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A Multiplex PCR-Based Next-Generation Sequencing Approach Has Detected a Common Large Deletion in STS Gene in a Patient With X-Linked Ichthyosis
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Obesity in Adults With 22q11.2 Deletion Syndrome
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