12 results on '"Zen, Paulo Ricardo Gazzola"'
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2. Trisomy 21 and Ebstein Anomaly: Diagnosis and Prognosis of a Rare Association
3. Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil
4. Microarray-Based Comparative Genomic Hybridization, Multiplex Ligation-Dependent Probe Amplification, and High-Resolution Karyotype for Differential Diagnosis Oculoauriculovertebral Spectrum: A Systematic Review
5. Unusual Characteristics and Variable Expressivity in a Brazilian Family with Cherubism
6. Pseudohypoparathyroidism with Ectopic Calcification and 22q11 Deletion Syndrome: A Rare Case
7. Ophthalmologic Impairment and Intellectual Disability in a Girl Presenting Kenny-Caffey Syndrome Type 2
8. Report of the Phenotype of a Patient with Roberts Syndrome and a Rare ESCO2 Variant
9. Trisomy 21 and Ebstein Anomaly: Diagnosis and Prognosis of a Rare Association
10. Unusual Characteristics and Variable Expressivity in a Brazilian Family with Cherubism
11. Pseudohypoparathyroidism with Ectopic Calcification and 22q11 Deletion Syndrome: A Rare Case
12. Report of the Phenotype of a Patient with Roberts Syndrome and a Rare ESCO2 Variant
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