A. Beaudet

发表

Microarray-based comparative genomic hybridization testing in deletion-bearing Angelman Syndrome patients: Genotype-phenotype correlations.

C. Bacino, T. Sahoo, S. Peters, 2005 .

Arginine-mediated regulation of an argininosuccinate synthetase minigene in normal and canavanine-resistant human cells

W. O'Brien, A. Beaudet, M. J. Jackson, 1986 .

The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications

P. Stankiewicz, S. Lalani, M. Shinawi, 2016, Journal of Autism and Developmental Disorders.

A fine structure physical map of the short arm of chromosome 5.

J. Wasmuth, J. Overhauser, A. Beaudet, 1986, American journal of human genetics.

A highly polymorphic locus in 5p15.2-5p15.3 (213-274EC) revealed by an anonymous single copy DNA fragment.

J. Wasmuth, J. Overhauser, A. Beaudet, 1987, Nucleic acids research.

Genomic evolution of epitopes and Low Complexity Regions in Plasmodium

H. Piontkivska, F. Battistuzzi, Sarah Medley, 2021, bioRxiv.

Heterogeneity of mutations in argininosuccinate synthetase causing human citrullinemia.

A. Beaudet, W. O'Brien, K. Kobayashi, 1990, The Journal of biological chemistry.

Deletion Syndrome : Clinical and Molecular Analysis Using Array CGH

Z. Ou, P. Stankiewicz, Ankita Patel, 2010 .

Denaturing high-performance liquid chromatography for the detection of mutations and polymorphisms in UBE3A.

A. Beaudet, D. Bercovich, A. Beaudet, 2003, Genetic testing.

Deletion Syndrome : Clinical and Molecular Analysis Using Array CGH

Z. Ou, P. Stankiewicz, S. Cheung, 2010 .

Metabolite regulation of argininosuccinate synthetase in cultured human cells.

A. Beaudet, W. O'Brien, S. Allen, 1988, The Journal of biological chemistry.