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Magnetic Resonance Imaging|March 1, 1989
In vivo muscle magnetic resonance spectroscopy in a family with mitochondrial cytopathy: a defect in fat metabolismP A Narayana, J M Slopis, E F Jackson, et al.The Journal of Rheumatology|April 1, 1993
Inflammatory arthropathies in children with chromosomal abnormalitiesD H Ihnat, G McIlvain-Simpson, K Conard, et al.Developmental Medicine and Child Neurology|January 1, 1994
The spasmodic upper-body squeeze: a characteristic behavior in Smith-Magenis syndromeB M Finucane, D Konar, B Haas-Givler, et al.American Journal of Medical Genetics|February 15, 1993
Eye abnormalities in the Smith-Magenis contiguous gene deletion syndromeB M Finucane, E R Jaeger, M B Kurtz, et al.American Journal of Medical Genetics|May 3, 1996
Sponastrime dysplasia: five new cases and review of nine previously published casesL O Langer, R K Beals, S LaFranchi, et al.American Journal of Medical Genetics|November 11, 1996
Extending the spectrum of distal arthrogryposisK W Gripp, C I Scott, B C Brockett, et al.American Journal of Medical Genetics. Part A|September 4, 2007
Weight for age charts for children with achondroplasiaJ E Hoover-Fong, J McGready, K J Schulze, et al.American Journal of Medical Genetics|November 1, 1992
Exclusion of human proteoglycan link protein (CRTL1) and type II collagen (COL2A1) genes in pseudoachondroplasiaJ T Hecht, S H Blanton, Y Wang, et al.Nature Genetics|April 16, 1998
Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathiesL E Warner, P Mancias, I J Butler, et al.Annals of Neurology|January 1, 1989
Cerebrospinal fluid biogenic amines and biopterin in Rett syndromeH Y Zoghbi, S Milstien, I J Butler, et al.Pageof 21