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	1.	Analysis of the VCX3A, VCX2 and VCX3B genes shows that VCX3A gene deletion is not sufficient to result in mental retardation in X-linked ichthyosis. [electronic resource] by Cuevas-Covarrubias, S A González-Huerta, L M Producer: 20080428 In: The British journal of dermatology vol. 158 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Segregation analysis in X-linked ichthyosis: paternal transmission of the affected X-chromosome. [electronic resource] by Toral-Lopez, J González-Huerta, L M Cuevas-Covarrubias, S A Producer: 20080807 In: The British journal of dermatology vol. 158 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Novel missense mutation (Arg432Cys) in a patient with steroid sulphatase-deficiency. [electronic resource] by González-Huerta, L M Riviera-Vega, M R Kofman-Alfeuro, S H Cuevas-Covarrubias, S A Producer: 20031009 In: Clinical endocrinology vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	[Hereditary sensory and autonomic neuropathy type II A: early neurological and skeletal findings]. [electronic resource] by Esmer, C Díaz Zambrano, S Santos Díaz, M A González Huerta, L M Cuevas Covarrubias, S A Bravo Oro, A Producer: 20150709 In: Anales de pediatria (Barcelona, Spain : 2003) vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Hereditary sensory and autonomic neuropathy II due to novel mutation in the HSN2 gene in Mexican families. [electronic resource] by Pacheco-Cuellar, G González-Huerta, L M Valdés-Miranda, J M Peláez-González, H Zenteno-Bacheron, S Cazarin-Barrientos, J Cuevas-Covarrubias, S A Producer: 20120123 In: Journal of neurology vol. 258 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A novel association in a family with oculo-auriculo-vertebral spectrum and x-linked ichthyosis. [electronic resource] by Rivera-Vega, M R Dueñas, Ernesto Jimenez-Vaca, A L Valdes-Flores, M Gonzalez-Huerta, L M Kofman-Alfaro, S H Cuevas-Covarrubias, S A Producer: 20030723 In: Pediatric dermatology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Deletion pattern of the STS gene in X-linked ichthyosis in a Mexican population. [electronic resource] by Jimenez Vaca, A L Valdes-Flores, M del R Rivera-Vega, M R González-Huerta, L M Kofman-Alfaro, S H Cuevas-Covarrubias, S A Producer: 20020712 In: Molecular medicine (Cambridge, Mass.) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	8.	Molecular analysis of the CYP1B1 gene: identification of novel truncating mutations in patients with primary congenital glaucoma. [electronic resource] by Messina-Baas, O M González-Huerta, L M Chima-Galán, C Kofman-Alfaro, S H Rivera-Vega, M R Babayán-Mena, I Cuevas-Covarrubias, S A Producer: 20070301 In: Ophthalmic research vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)