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Journal of Medical Genetics|March 15, 2011
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinomaBetty Gardie, Audrey Remenieras, Darouna Kattygnarath, et al.Journal of Medical Genetics|February 25, 1998
Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3S Olschwang, D Markie, S Seal, et al.Journal of Medical Genetics|February 25, 1998
Distal 10q trisomy syndrome with unusual cardiac and pulmonary abnormalitiesJ Davies, A Jaffé, A BushJournal of Medical Genetics|October 1, 1978
Familial atypical multiple mole-melanoma syndromeH T Lynch, B C Frichot, J F LynchJournal of Medical Genetics|October 1, 1978
The phenotype Ae1B: a probable result of chimerismG H Longster, E A Robinson, D I NorthJournal of Medical Genetics|October 1, 1978
Absent left hemidiaphragm, arhinencephaly, and cardiac malformationsN Fitch, H Srolovitz, Y Robitaille, et al.Journal of Medical Genetics|June 1, 1980
Ichthyosis, hepatosplenomegaly, and cerebellar degeneration in a sibshipP S Harper, R Marks, P J Dykes, et al.Journal of Medical Genetics|June 1, 1980
Gonadal dysgenesis in a patient with an X;3 translocation: case report and reviewN J Carpenter, B Say, D BrowningJournal of Medical Genetics|June 1, 1980
Tetrasomy 9p: confirmation by enzyme analysisS J Moedjono, B F Crandall, R S SparkesJournal of Medical Genetics|June 1, 1980
Partial trisomy of the short arm of chromosome 8 resulting from balanced maternal translocationL A Jones, D R Dengler, K Taysi, et al.Pageof 649