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You searched for: Author/Creator Lezirovitz, Karina

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1. A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58. (27th April 2020)

2. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. Issue 2 (6th December 2011)

3. Exome Sequencing Identifies a Novel Nonsense Mutation of MYO6 as the Cause of Deafness in a Brazilian Family. (17th October 2017)

4. Novel partial duplication of EYA1 causes branchiootic syndrome in a large Brazilian family. (September 2015)

5. Polyethylene glycol fusion associated with antioxidants: A new promise in the treatment of traumatic facial paralysis. Issue 7 (9th March 2018)

6. Polyethylene Glycol fusion associated with anti‐oxidants: A new promise in the treatment of traumatic paralysis. Issue 12 (28th December 2018)