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Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
October 1, 1976
[A contribution of new cytogenetic techniques to the knowledge of chromosomal abnormalities (author's transl)]
F Salamanca-Gómez, S Armendares
Annales De Genetique
|
December 1, 1975
Identification of isochromosome 17 in a girl with mental retardation and congenital malformations
F Salamanca-Gómez, S Armendares
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
October 1, 1975
[Lower lip and cleft lip with "pits" (Van der Woude syndrome). Study in a family (author's transl)]
J Guízar-Vázquez, S Armendares
Clinical Genetics
|
January 1, 1978
Partial 2p trisomy (p21 leads to pter) in two siblings of a family with a 2p-:15q+ translocation
S Armendares, F Salamanca-Gómez
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
July 1, 1973
[Differential diagnosis of congenital osteochondrodysplasia]
I Rostenberg, M Jiménez, S Armendares
Gaceta Medica De Mexico
|
April 1, 1974
[Current status of the knowledge of the effect of malnutrition on the genetic material]
S Armendares, F Salamanca, S Frenk
Gaceta Medica De Mexico
|
July 1, 1978
[Survey on the training in human sexuality matters required in medical schools of the Mexican Republic]
E Brostein de Ranen, S Armendares
Nature
|
July 23, 1971
Chromosome abnormalities in severe protein calorie malnutrition
S Armendares, F Salamanca, S Frenk
Annales De Genetique
|
September 1, 1972
Ring D 1 chromosome with remarkable morphological variation in a boy with mental retardation
F Salamanca, L Buentello, S Armendares
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
Page
of 11
Search research articles
Search
Showing results (21-30 of 103) with videos related to
Sort By:
Page
of 11
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
October 1, 1976
[A contribution of new cytogenetic techniques to the knowledge of chromosomal abnormalities (author's transl)]
F Salamanca-Gómez, S Armendares
Annales De Genetique
|
December 1, 1975
Identification of isochromosome 17 in a girl with mental retardation and congenital malformations
F Salamanca-Gómez, S Armendares
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
October 1, 1975
[Lower lip and cleft lip with "pits" (Van der Woude syndrome). Study in a family (author's transl)]
J Guízar-Vázquez, S Armendares
Clinical Genetics
|
January 1, 1978
Partial 2p trisomy (p21 leads to pter) in two siblings of a family with a 2p-:15q+ translocation
S Armendares, F Salamanca-Gómez
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
July 1, 1973
[Differential diagnosis of congenital osteochondrodysplasia]
I Rostenberg, M Jiménez, S Armendares
Gaceta Medica De Mexico
|
April 1, 1974
[Current status of the knowledge of the effect of malnutrition on the genetic material]
S Armendares, F Salamanca, S Frenk
Gaceta Medica De Mexico
|
July 1, 1978
[Survey on the training in human sexuality matters required in medical schools of the Mexican Republic]
E Brostein de Ranen, S Armendares
Nature
|
July 23, 1971
Chromosome abnormalities in severe protein calorie malnutrition
S Armendares, F Salamanca, S Frenk
Annales De Genetique
|
September 1, 1972
Ring D 1 chromosome with remarkable morphological variation in a boy with mental retardation
F Salamanca, L Buentello, S Armendares
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
Page
of 11