S. Armendares

发表

C bands in human metaphase chromosomes treated by barium hydroxide.

F. Salamanca, S. Armendares, 1974, Annales de genetique.

Gene frequencies and admixture estimates in a Mexico City population.

J. Granados, R. Lisker, S. Armendares, 1986, American journal of physical anthropology.

Two male sibs with uterus and Fallopian tubes. A rare, probably inherited disorder

S. Armendares, S. Frenk, L. Buentello, 1973, Clinical genetics.

Defective Monocyte Chemotaxis in Children with Down's Syndrome

R. Kretschmer, F. Salamanca, S. Armendares, 1983, Pediatric Research.

Chromosome Abnormalities in Severe Protein Calorie Malnutrition

F. Salamanca, S. Armendares, S. Frenk, 1971, Nature.

Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).

A. Carnevale, J. Cantú, F. Salamanca, 1975, Annales de genetique.

A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome.

F. Salamanca, S. Armendares, L. Buentello, 1972, Journal of medical genetics.

Histopathologic study with cytogenetic correlation in 20 cases of gonadal dysgenesis.

S. Armendares, H. Márquez-Monter, L. Buentello, 1972, American journal of clinical pathology.

Familial Occurrence of Persistent Müllerian Structures in Otherwise Normal Males

S. Najjar, A. Prader, M. Slim, 1973, British medical journal.

Familial true hermaphorodism in three siblings: plasma hormonal profile and in vitro steroid biosynthesis in gonadal structures.

N. Bedolla, V. Cortes-gallegos, S. Armendares, 1976, The Journal of clinical endocrinology and metabolism.

Partial 2p trisomy (p21→pter) in two siblings of a family with a 2p‐:15q+ translocation

F. Salamanca-Gómez, S. Armendares, 1978 .

The 12p trisomy syndrome.

J. Cantú, F. Salamanca, S. Armendares, 1975, Annales de genetique.

Attitudes of Mexican geneticists towards prenatal diagnosis and selective abortion.

A. Carnevale, A. Villa, R. Lisker, 1998, American journal of medical genetics.

Leukocyte function in Down's syndrome quantitative NBT reduction and bactericidal capacity

R. Kretschmer, S. Armendares, M. López‐Osuna, 1974 .

Ring chromosome 6 in a malformed boy

S. Armendares, Fabio Salamanca‐Gonez, Sara Nava, 1975, Clinical genetics.

Intrafamilial correlation analysis for IgM serum levels.

S. Armendares, I. Rostenberg, F. Saint-Martin, 1977, American journal of human genetics.

[Smith-Lemli-Opitz syndrome: description of 2 affected brothers, clinical characterization and hereditary mechanism].

A. Carnevale, V. del Castillo, S. Armendares, 1973, Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion.

Familial true hermaphrodism in three siblings

J. Cantú, V. Cortes-gallegos, F. Salamanca, 1975, Humangenetik.

[Clinical and cytogenetic findings in 74 patients with Turner's syndrome seen in a pediatric hospital (author's transl)].

F. Salamanca, S. Armendares, 1977, Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion.

Histidinaemia in a consanguineous marriage

S. Armendares, I. Rostenberg, I. Alejandre, 1974, Journal of medical genetics.

[Cp trisomy: a new syndrome].

S. Armendares, L. Buentello, J. Canu, 1971, Annales de genetique.

Ring D 1 chromosome with remarkable morphological variation in a boy with mental retardation.

F. Salamanca, S. Armendares, L. Buentello, 1972, Annales de genetique.

Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II.

F. Hecht, R. Magenis, R. Weleber, 1972, Annales de genetique.

Partial monosomy of a G group chromosome (45,XY,G-46,XY,Gr): report of a new case.

S. Armendares, L. Buentello, J. M. Cantú-Garza, 1971, Annales de genetique.

Familial extra centric bisatellited chromosome.

S. Armendares, L. Buentello, J. M. Cantú-Garza, 1969, Cytogenetics.

Letter: Absence of pectoralis major muscle in two sisters associated with leukemia in one of them.

S. Armendares, 1974, The Journal of pediatrics.

Microtia and meatal atresia in mother and son

F. Arredondo-Vega, S. Armendares, I. Rostenberg, 1978, Clinical genetics.

Mexican geneticists' opinions on disclosure issues.

A. Carnevale, D. Wertz, R. Lisker, 1999, Clinical genetics.

Frequency of sister chromatid exchanges in severe protein calorie malnutrition.

O. Mutchinick, R. Lisker, F. Salamanca, 1979, Annales de genetique.

A patient with 44 chromosomes.

F. Salamanca, S. Armendares, L. Buentello, 1985, Annales de genetique.

XO/XX/XXX MOSAICISM WITHOUT TURNER STIGMATA

S. Armendares, L. Buentello, J. Sánchez, 1967 .

Identification of isochromosome 17 in a girl with mental retardation and congenital malformations.

F. Salamanca-Gómez, S. Armendares, 1975, Annales de genetique.

Mexican geneticists’ views of ethical issues in genetics testing and screening. Are eugenic principles involved?

A. Carnevale, R. Lisker, S. Armendares, 1999, Clinical genetics.

Absence of correlation between Y chromosome heterochromatin and several anthropometric measurements in a Mexican population

O. Mutchinick, S. Armendares, L. Buentello, 2004, Human Genetics.

Human acrocentric ring chromosomes and satellite association.

J. Cantú, F. Salamanca, S. Armendares, 1975, Annales de genetique.

Iliac index in newborns. Comparative values at term, in prematurity, and in Down's syndrome.

S. Armendares, J. Urrusti-Sanz, E. Diaz-del-Castillo, 1967, American journal of diseases of children.

Potential fertility in incomplete male pseudohermaphroditism type 2.

J. Cantú, V. del Castillo, S. Armendares, 1976, Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion.