DNA deletion associated with hereditary neuropathy with liability to pressure palsies von Chance, Phillip F., Alderson, Mary Kathryn, Leppig, Kathleen A., Lensch, M.William, Matsunami, Norisada, Smith, Brooke, Swanson, Phillip D., Odelberg, Shannon J., Disteche, Christine M., Bird, Thomas D.

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Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17 von Chance, Phillip F., Abbas, Nacer, Lensch, M.William, Pentao, Liu, Roa, Benjamin B., Patel, Pragna I., Lupski, James R.

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Analysis of the CMT1A-REP repeat: mapping crossover breakpoints in CMT1A and HNPP von Kiyosawa, Hidenori, Lensch, M.William, Chance, Phillip F.

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The Fanconi anemia group C gene product von Fagerlie, Sara, Lensch, M.William, Pang, Qishen, Bagby, Grover C

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The Fanconi anemia group C gene product: Signaling functions in hematopoietic cells von Fagerlie, Sara, Lensch, M.William, Pang, Qishen, Bagby, Grover C

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