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Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disability

Clinical genetics, 2018-06, Vol.93 (6), p.1229-1233

2018

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Phosphodiesterase 8B Gene Variants Are Associated with Serum TSH Levels and Thyroid Function

American journal of human genetics, 2008-06, Vol.82 (6), p.1270-1280

2008

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Crouzon with acanthosis nigricans. Further delineation of the syndrome

Clinical genetics, 2007-11, Vol.72 (5), p.405-410

2007

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Políticas públicas y educación. Perspectiva latinoamericana desde el contexto de República Dominicana

Iustitia Socialis, 2022-11, Vol.7 (1), p.683

2022

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An aza-nucleoside, fragment-like inhibitor of the DNA repair enzyme alkyladenine glycosylase (AAG)

Bioorganic & medicinal chemistry, 2020-06, Vol.28 (11), p.115507-115507, Article 115507

2020

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Association between the Xba I Polymorphism of APOB Gene and Plasma Lipid Level in Mexican Patients with Coronary Artery Disease

Asia Pacific Journal of Clinical Nutrition, 2012-01, Vol.21 (2), p.312-318

2012

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Cytochrome P4501A1 polymorphism is associated with susceptibility to acute lymphoblastic leukemia in adult Mexican patients

Blood cells, molecules, & diseases, 2004-11, Vol.33 (3), p.326-329

2004

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First case reported of Turner syndrome and trisomy 14 chromosomal mosaicism in a patient

Clinical dysmorphology, 2008-01, Vol.17 (1), p.27-30

2008

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GSTT1 gene deletion is associated with lung cancer in Mexican patients

Disease markers, 2003-01, Vol.19 (6), p.259-261

2003

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Haplotypes Eco47 III– Nsp I sites frequencies on the IDUA gene in Mexican native population

European journal of medical genetics, 2005, Vol.48 (1), p.29-32

2005

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GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome

Hematology (Luxembourg), 2017-09, Vol.22 (8), p.467-5

2017

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Une nouvelle dynamique des solidarités dans le département des Hauts-de-Seine depuis juillet 2019

Regards, 2020-03, Vol.N° 56 (2), p.67-80

2020

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A highly complex rea(2;3;11) and aniridia by position effect

Cytogenetic and genome research, 2006-01, Vol.114 (1), p.83-88

2006

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Agenesis of the vocal cords in a female infant with Robin sequence

Clinical dysmorphology, 2011-10, Vol.20 (4), p.232-233

2011

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Influencia del microbioma intestinal en los trastornos neuropsiquiátricos: una revisión sistemática

Revista Ciencias Básicas en Salud, 2024-05, Vol.2 (2), p.12-34

Arnaud López, Lisset Josefina

2024

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Association between the Xba i polymorphism of APOB gene and plasma lipid level in Mexican patients with coronary artery disease

Asia Pacific journal of clinical nutrition, 2012-01, Vol.21 (2), p.312-318

2012

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Phosphodiesterese 8B Gene Variants Are Associated with Serum TSH Levels and Thyroid Function

American journal of human genetics, 2008-06, Vol.82 (6), p.1270

2008

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Ambiguous genitalia by 9p deletion inherent to a dic(Y;9)(q12;p24)

Journal of applied genetics, 2005, Vol.46 (4), p.415-418

2005

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Mapeo de las vías neuronales del estrés: una investigación psico química

Revista Ciencias Básicas en Salud, 2023-11, Vol.1 (2), p.26-45

2023

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Arterial hypertension and erectile dysfunction: an experience in the study of their comprehensive care

Salud, Ciencia y Tecnología - Serie de Conferencias, 2023-10, Vol.2, p.476

2023

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Mucopolysaccharidosis I: a comparative study of haplotypes Eco47III– NspI sites frequencies in patients and healthy subjects of Mexican population

Annales de génétique, 2003, Vol.46 (1), p.7-10

2003

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GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome

Hematology, 2017, Vol.22 (8), p.467-471

2017

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Systematic review of magnetic resonance imaging for diagnosis of Meniere disease

Journal of vestibular research, 2019-01, Vol.29 (2-3), p.121-129

2019

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Evolutionary Computation in Combinatorial Optimization: 18th European Conference, EvoCOP 2018, Parma, Italy, April 4-6, 2018, Proceedings

1, 2018

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Fabrication of PLA/PCL/Graphene Nanoplatelet (GNP) Electrically Conductive Circuit Using the Fused Filament Fabrication (FFF) 3D Printing Technique

Materials, 2022-01, Vol.15 (3), p.762

2022

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Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disability

Phosphodiesterase 8B Gene Variants Are Associated with Serum TSH Levels and Thyroid Function

Crouzon with acanthosis nigricans. Further delineation of the syndrome

Políticas públicas y educación. Perspectiva latinoamericana desde el contexto de República Dominicana

An aza-nucleoside, fragment-like inhibitor of the DNA repair enzyme alkyladenine glycosylase (AAG)

Association between the Xba I Polymorphism of APOB Gene and Plasma Lipid Level in Mexican Patients with Coronary Artery Disease

Cytochrome P4501A1 polymorphism is associated with susceptibility to acute lymphoblastic leukemia in adult Mexican patients

First case reported of Turner syndrome and trisomy 14 chromosomal mosaicism in a patient

GSTT1 gene deletion is associated with lung cancer in Mexican patients

Haplotypes Eco47 III– Nsp I sites frequencies on the IDUA gene in Mexican native population

GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome

Une nouvelle dynamique des solidarités dans le département des Hauts-de-Seine depuis juillet 2019

A highly complex rea(2;3;11) and aniridia by position effect

Agenesis of the vocal cords in a female infant with Robin sequence

Influencia del microbioma intestinal en los trastornos neuropsiquiátricos: una revisión sistemática

Association between the Xba i polymorphism of APOB gene and plasma lipid level in Mexican patients with coronary artery disease

Phosphodiesterese 8B Gene Variants Are Associated with Serum TSH Levels and Thyroid Function

Ambiguous genitalia by 9p deletion inherent to a dic(Y;9)(q12;p24)

Mapeo de las vías neuronales del estrés: una investigación psico química

Arterial hypertension and erectile dysfunction: an experience in the study of their comprehensive care

Mucopolysaccharidosis I: a comparative study of haplotypes Eco47III– NspI sites frequencies in patients and healthy subjects of Mexican population

GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome

Systematic review of magnetic resonance imaging for diagnosis of Meniere disease

Evolutionary Computation in Combinatorial Optimization: 18th European Conference, EvoCOP 2018, Parma, Italy, April 4-6, 2018, Proceedings

Fabrication of PLA/PCL/Graphene Nanoplatelet (GNP) Electrically Conductive Circuit Using the Fused Filament Fabrication (FFF) 3D Printing Technique

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