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Pediatric Radiology|January 1, 1986
Severe craniofacial sclerosis with multiple anomalies in a boy and his motherG Currarino, J M Friedman
Proceedings of the National Academy of Sciences of the United States of America|August 18, 1999
Leptin receptor activation of SH2 domain containing protein tyrosine phosphatase 2 modulates Ob receptor signal transductionC Li, J M Friedman
Computers and Biomedical Research, an International Journal|April 1, 1990
Interpreting chromosomal abnormalities using PrologG Cooper, J M Friedman
Pediatric Neurology|September 6, 2002
Unidentified bright objects associated with features of neurofibromatosis 1Jacek Szudek, J M Friedman
Clinical Genetics|November 15, 2002
Pathogenesis of hereditary tumors: beyond the "two-hit" hypothesisT Tucker, J M Friedman
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 3, 2004
Utility and limitations of genetic disease databases in clinical genetics research: a neurofibromatosis 1 database examplePatricia Birch, J M Friedman
Annals of Human Genetics|October 1, 1989
Analysing rearrangement breakpoint distributions by means of binomial confidence intervalsK Vasarhelyi, J M Friedman
Hematology/Oncology Clinics of North America|December 1, 1989
Local therapy of invasive diseaseJ Boyages, J R Harris
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