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Human Mutation|January 1, 1992
Illegitimate transcription: its use in the study of inherited diseaseJ C Kaplan, A Kahn, J Chelly
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1979
[Clinical and biological forms of cytochrome b5 reductase deficiency]J C Kaplan, A Leroux, P Beauvais
Human Molecular Genetics|January 1, 1993
Ten novel mutations in the HEXA gene in non-Jewish Tay-Sachs patientsS Akli, J C Chomel, J M Lacorte, et al.
The American Journal of Pediatric Hematology/Oncology|January 1, 1981
Glucocorticoid receptors in the lymphoblasts of patients with glucocorticoid-resistant childhood acute lymphocytic leukemiaR J Wells, K Mascaro, P C Young, et al.
The Journal of Biological Chemistry|August 5, 1986
In vivo developmental modifications of the expression of genes encoding muscle-specific enzymes in ratF Schweighoffer, P Maire, D Tuil, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 2, 1979
Study of a case with severe red-cell pyrimidine 5'-nucleotidase deficiencyH A Buc, J C Kaplan, A Najman
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