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Neurology|February 13, 2008
The molar tooth sign: a new Joubert syndrome and related cerebellar disorders classification system tested in Egyptian familiesM S Zaki, A Abdel-Aleem, G Abdel-Salam, et al.
Archives of Pathology & Laboratory Medicine|October 1, 1990
Neonatal intracranial choriocarcinomaS A Chandra, E F Gilbert, C Viseskul, et al.
American Journal of Nephrology|September 1, 1983
Secondary oxalosis as a complication of parenteral alimentation in acute renal failureA L Friedman, R W Chesney, E F Gilbert, et al.
Pediatric Radiology|January 1, 1982
Congenital generalized fibromatosis. Case report and literature reviewP W Brill, D R Yandow, L O Langer, et al.
The Annals of Thoracic Surgery|August 1, 1984
Total lymphatic irradiation and bone marrow in human heart transplantationD R Kahn, R Hong, A J Greenberg, et al.
American Journal of Diseases of Children (1960)|November 1, 1984
Renal-nonresponsive, bone-responsive pseudohypoparathyroidism. A case with normal vitamin D metabolite levels and clinical features of ricketsS Dabbagh, R W Chesney, L O Langer, et al.
American Journal of Medical Genetics|January 1, 1979
Mutations affecting pigmentation in man: I. Neuroectodermal melanolysosomal diseaseB R Elejalde, J Holguin, A Valencia, et al.
Human Molecular Genetics|November 18, 1998
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformationD T Pilz, N Matsumoto, S Minnerath, et al.
American Journal of Medical Genetics|February 13, 1995
Proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H): a model of a developmental field defectG Sorge, S Ardito, M Genuardi, et al.
American Journal of Medical Genetics|February 6, 1999
Previously apparently undescribed autosomal recessive MCA/MR syndrome with light fixation, retinal cone dystrophy, and seizures: the M syndromeA Rauch, K A Feindt, C O Leonard, et al.
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