Showing results (1-10 of 87) with videos related to

Sort By:
Pageof 9
Annales De Genetique|December 1, 1975
Identification of isochromosome 17 in a girl with mental retardation and congenital malformationsF Salamanca-Gómez, S Armendares
Clinical Genetics|January 1, 1978
Partial 2p trisomy (p21 leads to pter) in two siblings of a family with a 2p-:15q+ translocationS Armendares, F Salamanca-Gómez
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|July 1, 1990
[Cytogenetic study of the parents of 85 index cases with regular trisomy 21]S Armendares, L Buentello, F Salamanca
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|April 1, 1990
[Frequency of mixoploidy in 85 index cases with Down syndrome]S Armendares, L Buentellos, F Salamanca
Clinical Genetics|November 1, 1975
Ring chromosome 6 in a malformed boyF Salamanca-Gonez, S Nava, S Armendares
Archivos De Investigacion Medica|April 1, 1990
[Usefulness of chromosomal heteromorphisms obtained by G-banding for identification of illegitimacy]S Armendares, L Buentello, F Salamanca, et al.
Annales De Genetique|January 1, 1985
A patient with 44 chromosomesF Salamanca, L Buentello, J Sanchez, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|March 1, 1993
[Polymorphisms of chromosomes 1, 9, and 16 in Mexican mestizos]S Armendares, L Buentello, O Gaona, et al.
Annales De Genetique|January 1, 1979
Frequency of sister chromatid exchanges in severe protein calorie malnutritionO Mutchinick, R Lisker, L Ruz, et al.
Annales De Genetique|March 1, 1975
Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII)J M Cantu, F Salamanca, L Buentello, et al.
Pageof 9