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D Genís

Showing results (21-30 of 27) with videos related to

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Human Genetics|January 7, 1998
Polymorphisms at 13 expressed human sequences containing CAG/CTG repeats and analysis in autosomal dominant cerebellar ataxia (ADCA) patientsM A Pujana, M Gratacós, J Corral, et al.
Human Mutation|January 1, 1997
Sporadic heteroplasmic single 5.5 kb mitochondrial DNA deletion associated with cerebellar ataxia, hypogonadotropic hypogonadism, choroidal dystrophy, and mitochondrial respiratory chain complex I deficiencyA Barrientos, J Casademont, D Genís, et al.
Medicina Clinica|October 6, 1984
[Malignant syndrome caused by neuroleptics. A case produced by loxapine]D Genís Batlle, M Rubio Goday, J L González López, et al.
The Journal of Clinical Investigation|April 1, 1996
A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndromeA Barrientos, V Volpini, J Casademont, et al.
Neurology|September 3, 2010
Incidence and subtypes of early-onset dementia in a geographically defined general populationJ Garre-Olmo, D Genís Batlle, M del Mar Fernández, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|August 27, 2019
EXPLORATORY ANALYSIS OF RARE AND NOVEL VARIANTS IN MEXICAN PATIENTS DIAGNOSED WITH SCHIZOPHRENIA AND DEMENTIAJosé J Martínez-Magaña, Alma D Genís-Mendoza, Vanessa González-Covarrubias, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|October 11, 2019
EXPLORATORY ANALYSIS OF POLYGENIC RISK SCORES FOR PSYCHIATRIC DISORDERS: APPLIED TO DUAL DIAGNOSISJosé J Martínez-Magaña, Thelma B Gonzalez-Castro, Alma D Genís-Mendoza, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Human Genetics|January 7, 1998
Polymorphisms at 13 expressed human sequences containing CAG/CTG repeats and analysis in autosomal dominant cerebellar ataxia (ADCA) patientsM A Pujana, M Gratacós, J Corral, et al.
Human Mutation|January 1, 1997
Sporadic heteroplasmic single 5.5 kb mitochondrial DNA deletion associated with cerebellar ataxia, hypogonadotropic hypogonadism, choroidal dystrophy, and mitochondrial respiratory chain complex I deficiencyA Barrientos, J Casademont, D Genís, et al.
Medicina Clinica|October 6, 1984
[Malignant syndrome caused by neuroleptics. A case produced by loxapine]D Genís Batlle, M Rubio Goday, J L González López, et al.
The Journal of Clinical Investigation|April 1, 1996
A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndromeA Barrientos, V Volpini, J Casademont, et al.
Neurology|September 3, 2010
Incidence and subtypes of early-onset dementia in a geographically defined general populationJ Garre-Olmo, D Genís Batlle, M del Mar Fernández, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|August 27, 2019
EXPLORATORY ANALYSIS OF RARE AND NOVEL VARIANTS IN MEXICAN PATIENTS DIAGNOSED WITH SCHIZOPHRENIA AND DEMENTIAJosé J Martínez-Magaña, Alma D Genís-Mendoza, Vanessa González-Covarrubias, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|October 11, 2019
EXPLORATORY ANALYSIS OF POLYGENIC RISK SCORES FOR PSYCHIATRIC DISORDERS: APPLIED TO DUAL DIAGNOSISJosé J Martínez-Magaña, Thelma B Gonzalez-Castro, Alma D Genís-Mendoza, et al.
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