Lisa G. Shaffer

Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation.

L. Shaffer, K. Choo, S. Page, 1996, Human molecular genetics.

Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

L. Shaffer, W. Hul, C. Powell, 1996, American journal of human genetics.

DNA rearrangements on both homologues of chromosome 17 in a mildly delayed individual with a family history of autosomal dominant carpal tunnel syndrome.

L. Shaffer, J. Lupski, C. Kashork, 1999, American journal of human genetics.

Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH: implications for testing in the cytogenetics laboratory.

L. Shaffer, J. Lupski, A. Spikes, 1997, American journal of medical genetics.