2015 Year Book of Pediatrics. Ed. Cabana MD. (Elsevier; Philadelphia, PA)
Identification of Alu-mediated deletions in the Fanconi anemia gene FAA.
Disorders of DNA replication and repair.
Sequence variation in the Fanconi anemia gene FAA.
Stoichiometry of recombinant N-methyl-D-aspartate receptor channels inferred from single-channel current patterns.
Phenotypic consequences of mutations in the Fanconi anemia FAC gene: an International Fanconi Anemia Registry study.
Mutation in the M1 domain of the acetylcholine receptor alpha subunit decreases the rate of agonist dissociation.
The genomic organization of the Fanconi anemia group A (FAA) gene.
Interstitial lung disease in an adult with Fanconi anemia: clues to the pathogenesis.
Maximum likelihood estimation of aggregated Markov processes.
Subconductance states of a mutant NMDA receptor channel kinetics, calcium, and voltage dependence.
