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E Yunis

Showing results (11-20 of 105) with videos related to

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The Journal of Bone and Joint Surgery. American Volume|October 1, 1979
Fibrocartilaginous lesions of bone and hemangiomas and lipomas of soft tissue resembling Maffucci's syndrome. A case reportB L Bender, E Yunis
Journal of Medical Genetics|May 1, 1997
Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patientsH Arboleda, L Quintero, E Yunis
Clinical Genetics|October 1, 1980
X-linked Dyggve-Melchior-Clausen syndromeE Yunis, J Fontalvo, L Quintero
Human Genetics|January 1, 1981
Ring (15) chromosomeE Yunis, M Leibovici, L Quintero
Human Genetics|January 1, 1981
Duplication deficiency as the result of meiotic segregation of a maternal InV (10)E Yunis, O Torres de Caballero
Annales De Genetique|March 1, 1976
Trisomy iopE Yunis, R Silva, A Giraldo
Cancer Genetics and Cytogenetics|September 1, 1994
Phenotype variants, malignancy, and additional copies of 6p in retinoblastomaJ Cano, O Oliveros, E Yunis
Transplantation Proceedings|December 1, 1979
Suppression of the cytotoxic response (CML) in man by precultured cells: association with a monocyte/macrophage cell fractionD Dubey, S Stux, E Yunis
Human Genetics|January 1, 1981
Monosomy 1pterE Yunis, L Quintero, M Leibovici
Human Genetics|January 1, 1981
Retinoblastoma, gross internal malformations, and deletion 13q14 leads to q31E Yunis, R Zuñiga, E Ramírez
Pageof 11

Showing results (11-20 of 105) with videos related to

Sort By:
Pageof 11
The Journal of Bone and Joint Surgery. American Volume|October 1, 1979
Fibrocartilaginous lesions of bone and hemangiomas and lipomas of soft tissue resembling Maffucci's syndrome. A case reportB L Bender, E Yunis
Journal of Medical Genetics|May 1, 1997
Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patientsH Arboleda, L Quintero, E Yunis
Clinical Genetics|October 1, 1980
X-linked Dyggve-Melchior-Clausen syndromeE Yunis, J Fontalvo, L Quintero
Human Genetics|January 1, 1981
Ring (15) chromosomeE Yunis, M Leibovici, L Quintero
Human Genetics|January 1, 1981
Duplication deficiency as the result of meiotic segregation of a maternal InV (10)E Yunis, O Torres de Caballero
Annales De Genetique|March 1, 1976
Trisomy iopE Yunis, R Silva, A Giraldo
Cancer Genetics and Cytogenetics|September 1, 1994
Phenotype variants, malignancy, and additional copies of 6p in retinoblastomaJ Cano, O Oliveros, E Yunis
Transplantation Proceedings|December 1, 1979
Suppression of the cytotoxic response (CML) in man by precultured cells: association with a monocyte/macrophage cell fractionD Dubey, S Stux, E Yunis
Human Genetics|January 1, 1981
Monosomy 1pterE Yunis, L Quintero, M Leibovici
Human Genetics|January 1, 1981
Retinoblastoma, gross internal malformations, and deletion 13q14 leads to q31E Yunis, R Zuñiga, E Ramírez
Pageof 11