Jackson, Laird G
Children's Hospital of Philadelphia · Drexel University
3 papers on CoChat
Most cited papers
- Verified
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B
Krantz, I. D., McCallum, J., DeScipio, C., Kaur, M., Gillis, L. A., Yaeger, D., Jukofsky, L., Wasserman, N., Bottani, A., Morris, C. A., et al. (2004) · Nature Genetics
Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders
Cited by 713
- Verified
HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle
Deardorff, M. A., Bando, M., Nakato, R., Watrin, E., Itoh, T., Minamino, M., Saitoh, K., Komata, M., Katou, Y., Clark, D., et al. (2012) · Nature
Genomics and Chromatin DynamicsDNA Repair Mechanisms
Cited by 577
- Verified
Noninvasive prenatal diagnosis of fetal aneuploidies and Mendelian disorders: new innovative strategies
Hahn, S., Jackson, L. G., Kolla, V., Mahyuddin, A. P., & Choolani, M. (2009) · Expert Review of Molecular Diagnostics
Prenatal Screening and DiagnosticsCancer Genomics and Diagnostics
Cited by 32
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