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Molecular Biology Reports|June 18, 2022
CRISPR/Cas9 a simple, inexpensive and effective technique for gene editingPatrick Ferreira, Altino Branco ChoupinaJIMD Reports|February 22, 2017
Irreversibility of Symptoms with Biotin Therapy in an Adult with Profound Biotinidase DeficiencyPatrick Ferreira, Alicia Chan, Barry WolfOphthalmic Genetics|April 8, 2016
Oculomotor apraxia and dilated cardiomyopathy with ataxia syndrome: A case reportMatthew D Benson, Patrick Ferreira, Ian M MacDonaldPediatric Blood & Cancer|May 4, 2016
Severe Congenital Protein C Deficiency: Practical Aspects of ManagementRavi Shah, Patrick Ferreira, Shelina Karmali, et al.Plants (Basel, Switzerland)|November 25, 2023
Post-Transcriptional Gene Silencing of Glucanase Inhibitor Protein in Phytophthora cinnamomiPatrick Ferreira, Abdessalem Chahed, Letícia M Estevinho, et al.Neurology. Genetics|April 12, 2016
Late diagnosis of cerebral folate deficiency: Fewer seizures with folinic acid in adult siblingsPatrick Ferreira, Stephanie M Luco, Sarah L Sawyer, et al.Molecular Genetics and Metabolism|March 13, 2017
Hypertryptophanemia due to tryptophan 2,3-dioxygenase deficiencyPatrick Ferreira, Inchul Shin, Iveta Sosova, et al.Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 16, 2010
Gaucher disease with prenatal onset and perinatal death due to compound heterozygosity for the missense R131C and null Rec Nci I GBA mutationsApril Goebl, Raechel A Ferrier, Patrick Ferreira, et al.Blood Cells, Molecules & Diseases|January 2, 2007
Gaucher disease among Chinese patients: review on genotype/phenotype correlation from 29 patients and identification of novel and rare allelesFrancis Y M Choy, Weimin Zhang, Hui-Ping Shi, et al.American Journal of Medical Genetics. Part A|October 7, 2020
Congenital hiatal hernia segregating with a duplication in 9q22.31q22.32 in two familiesCaitlin A Chang, Nataliya Di Donato, Karl Hackmann, et al.Pageof 3