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C Sultan

Showing results (241-250 of 284) with videos related to

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British Journal of Haematology|March 1, 1984
Myelodysplastic syndromes: is another classification necessary?J M Bennett, D Catovsky, M T Daniel, et al.
British Journal of Haematology|January 1, 1980
A variant form of hypergranular promyelocytic leukaemia (M3)J M Bennett, D Catovsky, M T Daniel, et al.
International Journal of Andrology|February 6, 2010
Undervirilization in XY newborns may hide a 5α-reductase deficiency: report of three new SRD5A2 gene mutationsL Maimoun, P Philibert, B Cammas, et al.
Annales De Biologie Clinique|January 1, 1989
[Bioluminescence assay of luteinizing hormone in plasma and urine]B Terouanne, S Alameddine, J L Martin, et al.
British Journal of Haematology|August 1, 1994
The chronic myeloid leukaemias: guidelines for distinguishing chronic granulocytic, atypical chronic myeloid, and chronic myelomonocytic leukaemia. Proposals by the French-American-British Cooperative Leukaemia GroupJ M Bennett, D Catovsky, M T Daniel, et al.
Gynecologie, Obstetrique & Fertilite|January 3, 2009
[Juvenile granulosa-cell tumor: clinical and molecular expression]N Kalfa, P Philibert, C Patte, et al.
Human Reproduction Update|June 8, 2001
Disorders linked to insufficient androgen action in male childrenC Sultan, F Paris, B Terouanne, et al.
Journal of Endocrinological Investigation|June 1, 2010
The IVS1-2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiencyN Skordis, V Neocleous, A Kyriakou, et al.
Annales De Medecine Interne|November 1, 1976
[Developmental aspects of angioimmunoblastic lymphadenopathy. Apropos of 3 cases]H Rochant, F Reyes, J P Vernant, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
Molecular study of the 5 alpha-reductase type 2 gene in three European families with 5 alpha-reductase deficiencyC Boudon, S Lumbroso, J M Lobaccaro, et al.
Pageof 29

Showing results (241-250 of 284) with videos related to

Sort By:
Pageof 29
British Journal of Haematology|March 1, 1984
Myelodysplastic syndromes: is another classification necessary?J M Bennett, D Catovsky, M T Daniel, et al.
British Journal of Haematology|January 1, 1980
A variant form of hypergranular promyelocytic leukaemia (M3)J M Bennett, D Catovsky, M T Daniel, et al.
International Journal of Andrology|February 6, 2010
Undervirilization in XY newborns may hide a 5α-reductase deficiency: report of three new SRD5A2 gene mutationsL Maimoun, P Philibert, B Cammas, et al.
Annales De Biologie Clinique|January 1, 1989
[Bioluminescence assay of luteinizing hormone in plasma and urine]B Terouanne, S Alameddine, J L Martin, et al.
British Journal of Haematology|August 1, 1994
The chronic myeloid leukaemias: guidelines for distinguishing chronic granulocytic, atypical chronic myeloid, and chronic myelomonocytic leukaemia. Proposals by the French-American-British Cooperative Leukaemia GroupJ M Bennett, D Catovsky, M T Daniel, et al.
Gynecologie, Obstetrique & Fertilite|January 3, 2009
[Juvenile granulosa-cell tumor: clinical and molecular expression]N Kalfa, P Philibert, C Patte, et al.
Human Reproduction Update|June 8, 2001
Disorders linked to insufficient androgen action in male childrenC Sultan, F Paris, B Terouanne, et al.
Journal of Endocrinological Investigation|June 1, 2010
The IVS1-2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiencyN Skordis, V Neocleous, A Kyriakou, et al.
Annales De Medecine Interne|November 1, 1976
[Developmental aspects of angioimmunoblastic lymphadenopathy. Apropos of 3 cases]H Rochant, F Reyes, J P Vernant, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
Molecular study of the 5 alpha-reductase type 2 gene in three European families with 5 alpha-reductase deficiencyC Boudon, S Lumbroso, J M Lobaccaro, et al.
Pageof 29