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American Journal of Medical Genetics|December 8, 1998
Novel V184E MEN1 germline mutation in a Japanese kindred with familial hyperparathyroidismM Fujimori, S Shirahama, A Sakurai, et al.American Journal of Medical Genetics|December 8, 1998
Developmental delay and growth failure caused by a peroxisomal disorder, dihydroxyacetonephosphate acyltransferase (DHAP-AT) deficiencyE R Elias, M Mobassaleh, A K Hajra, et al.American Journal of Medical Genetics|December 8, 1998
Prader-Willi-like syndrome in a patient with an Xq23q25 duplicationK G Monaghan, D L Van Dyke, G L FeldmanAmerican Journal of Medical Genetics|December 8, 1998
Craniofacial variability index: a simple measure of normal and abnormal variation in the head and faceR E Ward, P L Jamison, L G FarkasAmerican Journal of Medical Genetics|December 8, 1998
Radiographic and morphologic findings in a previously undescribed type of mesomelic dysplasia resembling atelosteogenesis type IIS G Brodie, R S Lachman, B F Crandall, et al.American Journal of Medical Genetics|December 8, 1998
Methylation PCR analysis of Prader-Willi syndrome, Angelman syndrome, and control subjectsB Muralidhar, M G ButlerAmerican Journal of Medical Genetics|December 8, 1998
Short-rib-polydactyly syndrome type Verma-Naumoff-Le Marec in a fetus with histological hallmarks of type Saldino-Noonan but lacking internal organ abnormalitiesS Hentze, C Sergi, J Troeger, et al.American Journal of Medical Genetics|November 11, 1996
Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11)C A Walter, L G Shaffer, C I Kaye, et al.American Journal of Medical Genetics|November 11, 1996
Mortality in patients with acute intermittent porphyria requiring hospitalization: a United States case seriesJ B Jeans, K Savik, C R Gross, et al.American Journal of Medical Genetics|November 11, 1996
A revised and extended classification of the distal arthrogryposesM Bamshad, L B Jorde, J C CareyPageof 854