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S H Kofman-Alfaro

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Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|October 1, 1990
[The human Y chromosome]S A Cuevas-Covarrubias, S H Kofman-Alfaro
The Journal of Investigative Dermatology|March 7, 2001
Deletion of exons 1-5 of the STS gene causing X-linked ichthyosisM Valdes-Flores, S H Kofman-Alfaro, A L Vaca, et al.
The Journal of Investigative Dermatology|February 26, 2000
Mutation report: a novel partial deletion of exons 2-10 of the STS gene in recessive X-linked ichthyosisM Valdes-Flores, S H Kofman-Alfaro, A L Vaca, et al.
The Journal of Dermatology|September 1, 1996
Accuracy of the clinical diagnosis of recessive X-linked ichthyosis vs ichthyosis vulgarisS A Cuevas-Covarrubias, S H Kofman-Alfaro, A B Palencia, et al.
Clinical Genetics|October 1, 1996
Congenital heart defect and conductive hypoacusia in a patient with the KBG syndromeM R Rivera-Vega, N Leyva Juárez, S A Cuevas-Covarrubias, et al.
Acta Dermato-Venereologica|June 20, 2001
Characterization of a novel point mutation (Arg432His) in X-linked ichthyosisM Valdes-Flores, A L Jimenez Vaca, S H Kofman-Alfaro, et al.
American Journal of Medical Genetics|July 31, 2001
Carrier identification by FISH analysis in isolated cases of X-linked ichthyosisM Valdes-Flores, S H Kofman-Alfaro, A L Jimenez-Vaca, et al.
American Journal of Medical Genetics|December 31, 1997
X-linked ichthyosis in Mexico: high frequency of deletions in the steroid sulfatase encoding geneS A Cuevas-Covarrubias, S H Kofman-Alfaro, G Maya-Núñez, et al.
The Journal of Investigative Dermatology|October 26, 2001
Maternal transmission of the 3 bp deletion within exon 7 of the STS gene in steroid sulfatase deficiencyM Valdes-Flores, A L Vaca, M R Rivera-Vega, et al.
The Journal of Dermatology|October 14, 1998
Are atopy and palm-sole hyperlinearity clinical tools in the differential diagnosis between ichthyosis vulgaris and X-linked ichthyosis?S A Cuevas-Covarrubias, M Valdés-Flores, E Orozco Orozco, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|October 1, 1990
[The human Y chromosome]S A Cuevas-Covarrubias, S H Kofman-Alfaro
The Journal of Investigative Dermatology|March 7, 2001
Deletion of exons 1-5 of the STS gene causing X-linked ichthyosisM Valdes-Flores, S H Kofman-Alfaro, A L Vaca, et al.
The Journal of Investigative Dermatology|February 26, 2000
Mutation report: a novel partial deletion of exons 2-10 of the STS gene in recessive X-linked ichthyosisM Valdes-Flores, S H Kofman-Alfaro, A L Vaca, et al.
The Journal of Dermatology|September 1, 1996
Accuracy of the clinical diagnosis of recessive X-linked ichthyosis vs ichthyosis vulgarisS A Cuevas-Covarrubias, S H Kofman-Alfaro, A B Palencia, et al.
Clinical Genetics|October 1, 1996
Congenital heart defect and conductive hypoacusia in a patient with the KBG syndromeM R Rivera-Vega, N Leyva Juárez, S A Cuevas-Covarrubias, et al.
Acta Dermato-Venereologica|June 20, 2001
Characterization of a novel point mutation (Arg432His) in X-linked ichthyosisM Valdes-Flores, A L Jimenez Vaca, S H Kofman-Alfaro, et al.
American Journal of Medical Genetics|July 31, 2001
Carrier identification by FISH analysis in isolated cases of X-linked ichthyosisM Valdes-Flores, S H Kofman-Alfaro, A L Jimenez-Vaca, et al.
American Journal of Medical Genetics|December 31, 1997
X-linked ichthyosis in Mexico: high frequency of deletions in the steroid sulfatase encoding geneS A Cuevas-Covarrubias, S H Kofman-Alfaro, G Maya-Núñez, et al.
The Journal of Investigative Dermatology|October 26, 2001
Maternal transmission of the 3 bp deletion within exon 7 of the STS gene in steroid sulfatase deficiencyM Valdes-Flores, A L Vaca, M R Rivera-Vega, et al.
The Journal of Dermatology|October 14, 1998
Are atopy and palm-sole hyperlinearity clinical tools in the differential diagnosis between ichthyosis vulgaris and X-linked ichthyosis?S A Cuevas-Covarrubias, M Valdés-Flores, E Orozco Orozco, et al.
Pageof 2