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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 report
B L Bender, E Yunis
Journal of Medical Genetics
|
May 1, 1997
Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patients
H Arboleda, L Quintero, E Yunis
Clinical Genetics
|
October 1, 1980
X-linked Dyggve-Melchior-Clausen syndrome
E Yunis, J Fontalvo, L Quintero
Human Genetics
|
January 1, 1981
Ring (15) chromosome
E 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 iop
E Yunis, R Silva, A Giraldo
Cancer Genetics and Cytogenetics
|
September 1, 1994
Phenotype variants, malignancy, and additional copies of 6p in retinoblastoma
J 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 fraction
D Dubey, S Stux, E Yunis
Human Genetics
|
January 1, 1981
Monosomy 1pter
E Yunis, L Quintero, M Leibovici
Human Genetics
|
January 1, 1981
Retinoblastoma, gross internal malformations, and deletion 13q14 leads to q31
E Yunis, R Zuñiga, E Ramírez
Page
of 11
Search research articles
Search
Showing results (11-20 of 105) with videos related to
Sort By:
Page
of 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 report
B L Bender, E Yunis
Journal of Medical Genetics
|
May 1, 1997
Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patients
H Arboleda, L Quintero, E Yunis
Clinical Genetics
|
October 1, 1980
X-linked Dyggve-Melchior-Clausen syndrome
E Yunis, J Fontalvo, L Quintero
Human Genetics
|
January 1, 1981
Ring (15) chromosome
E 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 iop
E Yunis, R Silva, A Giraldo
Cancer Genetics and Cytogenetics
|
September 1, 1994
Phenotype variants, malignancy, and additional copies of 6p in retinoblastoma
J 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 fraction
D Dubey, S Stux, E Yunis
Human Genetics
|
January 1, 1981
Monosomy 1pter
E Yunis, L Quintero, M Leibovici
Human Genetics
|
January 1, 1981
Retinoblastoma, gross internal malformations, and deletion 13q14 leads to q31
E Yunis, R Zuñiga, E Ramírez
Page
of 11