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Vera Lúcia Gil da Silva Lopes

State University of Campinas

137

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An Overview of the Trajectory of Brazilian Individuals with 22q11.2 Deletion Syndrome Until Diagnosis.

2021
- Isabela Mayá Wayhs Silva
- Vera Lúcia Gil da Silva Lopes
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Further evidence for lack of association of PRDM9 polymorphisms and 22q11.2 deletion syndrome

2021 Meta Gene
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Craniofacial microsomia: Reflections on diagnosis and severity assessment based on a series of cases.

2021 Congenital Anomalies
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Trisomy X in a patient with childhood-onset systemic lupus erythematosus

2020
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Identification of genomic imbalances in oral clefts.

2020 Jornal De Pediatria
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Polimorfismos do gene IRF6 em pacientes brasileiros com fenda labial não sindrômica com ou sem fenda palatina

2020
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Brazil's Craniofacial Project: Different approaches on orofacial clefts and 22q11.2 deletion syndrome.

2020 American Journal of Medical Genetics Part C-seminars in Medical Genetics
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Genomic imbalances in craniofacial microsomia.

2020 American Journal of Medical Genetics Part C-seminars in Medical Genetics
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Testing criteria for 22q11.2 deletion syndrome: preliminary results of a low cost strategy for public health

2019 Orphanet Journal of Rare Diseases
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Obituary: Antonio Richieri‐Costa (1946–2019)

2019 American Journal of Medical Genetics Part A
- Vera Lúcia Gil da Silva Lopes
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