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Pediatric Radiology|January 1, 1986
Severe craniofacial sclerosis with multiple anomalies in a boy and his motherG Currarino, J M FriedmanProceedings 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 FriedmanClinical Genetics|September 14, 2007
The impact of array genomic hybridization on mental retardation research: a review of current technologies and their clinical utilityF Zahir, J M FriedmanComputers and Biomedical Research, an International Journal|April 1, 1990
Interpreting chromosomal abnormalities using PrologG Cooper, J M FriedmanPediatric Neurology|September 6, 2002
Unidentified bright objects associated with features of neurofibromatosis 1Jacek Szudek, J M FriedmanClinical Genetics|November 15, 2002
Pathogenesis of hereditary tumors: beyond the "two-hit" hypothesisT Tucker, J M FriedmanAmerican 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 FriedmanAnnals of Human Genetics|October 1, 1989
Analysing rearrangement breakpoint distributions by means of binomial confidence intervalsK Vasarhelyi, J M FriedmanGenome Research|September 29, 1998
Microsatellite marker content mapping of 12 candidate genes for obesity: assembly of seven obesity screening panels for automated genotypingJ D Winick, J M FriedmanCMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|August 21, 2002
Medical genetics: 1. Clinical teratology in the age of genomicsJanine E Polifka, J M FriedmanPageof 37