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Community Genetics
|
November 13, 2004
Genetic services in Mexico City
Susana Kofman-Alfaro, Juan Carlos Zenteno
Community Genetics
|
November 16, 2004
Community genetic services in Latin America and regional network of medical genetics. Recommendations of a World Health Organization consultation
Susana Kofman-Alfaro, Victor B Penchaszadeh
Archives of Gynecology and Obstetrics
|
June 29, 2004
Molecular analysis of the anti-Müllerian hormone, the anti-Müllerian hormone receptor, and galactose-1-phosphate uridyl transferase genes in patients with the Mayer-Rokitansky-Küster-Hauser syndrome
Juan Carlos Zenteno, Sebastian Carranza-Lira, Susana Kofman-Alfaro
Hormone Research
|
May 15, 2002
Phenotypic heterogeneity associated with identical mutations in residue 870 of the androgen receptor
Juan Carlos Zenteno, Bertha Chávez, Felipe Vilchis, et al.
American Journal of Medical Genetics. Part A
|
March 1, 2005
Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of TP63
Juan Carlos Zenteno, Valeria Berdón-Zapata, Susana Kofman-Alfaro, et al.
Journal of Human Genetics
|
August 9, 2003
Extreme androgen resistance in a kindred with a novel insertion/deletion mutation in exon 5 of the androgen receptor gene
Felipe Vilchis, Luis Ramos, Susana Kofman-Alfaro, et al.
Human Pathology
|
March 28, 2006
Extragonadal germ cell tumors are often associated with Klinefelter syndrome
David Aguirre, Karem Nieto, Minerva Lazos, et al.
American Journal of Medical Genetics. Part A
|
June 9, 2005
A novel filamin A D203Y mutation in a female patient with otopalatodigital type 1 syndrome and extremely skewed X chromosome inactivation
Alberto Hidalgo-Bravo, Ericka N Pompa-Mera, Susana Kofman-Alfaro, et al.
American Journal of Medical Genetics
|
January 25, 2002
Microsatellite analysis in Turner syndrome: parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes
Nancy Monroy, Marisol López, Alicia Cervantes, et al.
Cancer Letters
|
February 26, 2008
Participation of OCT3/4 and beta-catenin during dysgenetic gonadal malignant transformation
Icela Palma, Rocio-Yolanda Peña, Alejandra Contreras, et al.
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Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
Community Genetics
|
November 13, 2004
Genetic services in Mexico City
Susana Kofman-Alfaro, Juan Carlos Zenteno
Community Genetics
|
November 16, 2004
Community genetic services in Latin America and regional network of medical genetics. Recommendations of a World Health Organization consultation
Susana Kofman-Alfaro, Victor B Penchaszadeh
Archives of Gynecology and Obstetrics
|
June 29, 2004
Molecular analysis of the anti-Müllerian hormone, the anti-Müllerian hormone receptor, and galactose-1-phosphate uridyl transferase genes in patients with the Mayer-Rokitansky-Küster-Hauser syndrome
Juan Carlos Zenteno, Sebastian Carranza-Lira, Susana Kofman-Alfaro
Hormone Research
|
May 15, 2002
Phenotypic heterogeneity associated with identical mutations in residue 870 of the androgen receptor
Juan Carlos Zenteno, Bertha Chávez, Felipe Vilchis, et al.
American Journal of Medical Genetics. Part A
|
March 1, 2005
Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of TP63
Juan Carlos Zenteno, Valeria Berdón-Zapata, Susana Kofman-Alfaro, et al.
Journal of Human Genetics
|
August 9, 2003
Extreme androgen resistance in a kindred with a novel insertion/deletion mutation in exon 5 of the androgen receptor gene
Felipe Vilchis, Luis Ramos, Susana Kofman-Alfaro, et al.
Human Pathology
|
March 28, 2006
Extragonadal germ cell tumors are often associated with Klinefelter syndrome
David Aguirre, Karem Nieto, Minerva Lazos, et al.
American Journal of Medical Genetics. Part A
|
June 9, 2005
A novel filamin A D203Y mutation in a female patient with otopalatodigital type 1 syndrome and extremely skewed X chromosome inactivation
Alberto Hidalgo-Bravo, Ericka N Pompa-Mera, Susana Kofman-Alfaro, et al.
American Journal of Medical Genetics
|
January 25, 2002
Microsatellite analysis in Turner syndrome: parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes
Nancy Monroy, Marisol López, Alicia Cervantes, et al.
Cancer Letters
|
February 26, 2008
Participation of OCT3/4 and beta-catenin during dysgenetic gonadal malignant transformation
Icela Palma, Rocio-Yolanda Peña, Alejandra Contreras, et al.
Page
of 2