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Genomics|December 1, 1987
Regional mapping panel for human chromosome 17: application to neurofibromatosis type 1P van Tuinen, D C Rich, K M Summers, et al.American Journal of Human Genetics|January 1, 1989
Precise localization of NF1 to 17q11.2 by balanced translocationD H Ledbetter, D C Rich, P O'Connell, et al.Journal of Pediatric Surgery|February 1, 1997
Second malignant neoplasms in children after treatment of soft tissue sarcomaD C Rich, C A Corpron, M B Smith, et al.American Journal of Medical Genetics|September 1, 1988
Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomalyF Greenberg, K B Courtney, R A Wessels, et al.American Journal of Human Genetics|November 1, 1988
Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndromeP vanTuinen, W B Dobyns, D C Rich, et al.Genomics|August 1, 1990
The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocationsP O'Connell, D Viskochil, A M Buchberg, et al.Science (New York, N.Y.)|June 2, 1989
Two NF1 translocations map within a 600-kilobase segment of 17q11.2P O'Connell, R Leach, R M Cawthon, et al.Genomics|August 1, 1989
Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17A G Menon, D H Ledbetter, D C Rich, et al.American Journal of Human Genetics|January 1, 1989
Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17J W Fountain, M R Wallace, A M Brereton, et al.Pageof 1