Showing results (21-30 of 98) with videos related to
Sort By:
Pageof 10
American Journal of Diseases of Children (1960)|January 1, 1977
Renal anomalies and oligohydramnios in the cerebro-oculofacio-skeletal syndromeM Preus, P Kaplan, T H KirkhamJournal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|October 1, 1989
Serum isoenzyme pattern of creatine kinase and lactate dehydrogenase in various animal speciesM Preus, B Karsten, A S BhargavaClinical Genetics|July 1, 1984
Trisomy 9 (pter----q1 to q3): the phenotype as an objective aid to karyotypic interpretationM Preus, A Schinzel, S Aymé, et al.American Journal of Medical Genetics|June 1, 1985
A taxonomic approach to the del(4p) phenotypeM Preus, S Aymé, P Kaplan, et al.American Journal of Medical Genetics|January 1, 1981
Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly"F C Fraser, A LytwynJournal of Medical Genetics|December 1, 1982
Spectrum of anomalies in Fanconi anaemiaA Glanz, F C FraserAmerican Journal of Medical Genetics|March 4, 2000
Recurrence risk for sibs of children with "sporadic" achondroplasiaG Mettler, F C FraserJournal of Medical Genetics|June 1, 1977
Diabetes mellitus, diabetes insipidus, and optic atrophy. An autosomal recessive syndrome?F C Fraser, T GunnJournal of Medical Genetics|April 1, 1979
Camptodactyly, cleft palate, and club foot (the Gordon syndrome). A report of a large pedigreeF Halal, F C FraserPageof 10