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Plos One
|
May 25, 2013
PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data
Geòrgia Escaramís, Cristian Tornador, Laia Bassaganyas, et al.
Bone
|
May 27, 2022
Clinical description and genetic analysis of a novel familial skeletal dysplasia characterized by high bone mass and lucent bone lesions
Diana Ovejero, Natalia Garcia-Giralt, Núria Martínez-Gil, et al.
Journal of Medical Genetics
|
March 28, 2024
Subcellular localisation of truncated MAGEL2 proteins: insight into the molecular pathology of Schaaf-Yang syndrome
Mónica Centeno-Pla, Estefanía Alcaide-Consuegra, Sophie Gibson, et al.
Journal of Affective Disorders
|
February 18, 2020
Exploring genetic variants in obsessive compulsive disorder severity: A GWAS approach
María Alemany-Navarro, Raquel Cruz, Eva Real, et al.
Genes
|
January 21, 2022
Gene Network of Susceptibility to Atypical Femoral Fractures Related to Bisphosphonate Treatment
Natalia Garcia-Giralt, Neus Roca-Ayats, Josep F Abril, et al.
Pain
|
March 4, 2014
Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system
Elisa Docampo, Georgia Escaramís, Mònica Gratacòs, et al.
International Journal of Molecular Sciences
|
July 24, 2021
Functional Analyses of Four <i>CYP1A1</i> Missense Mutations Present in Patients with Atypical Femoral Fractures
Nerea Ugartondo, Núria Martínez-Gil, Mònica Esteve, et al.
International Journal of Molecular Sciences
|
February 9, 2021
<i>De Novo PORCN</i> and <i>ZIC2</i> Mutations in a Highly Consanguineous Family
Laura Castilla-Vallmanya, Semra Gürsoy, Özlem Giray-Bozkaya, et al.
Biochimica Et Biophysica Acta
|
November 26, 2008
Are MYO1C and MYO1F associated with hearing loss?
Cristina Zadro, Maria Stella Alemanno, Emanuele Bellacchio, et al.
Arthritis and Rheumatism
|
March 10, 2010
Deletion of the late cornified envelope genes, LCE3C and LCE3B, is associated with rheumatoid arthritis
Elisa Docampo, Raquel Rabionet, Eva Riveira-Muñoz, et al.
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of 7
Search research articles
Search
Showing results (21-30 of 63) with videos related to
Sort By:
Page
of 7
Plos One
|
May 25, 2013
PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data
Geòrgia Escaramís, Cristian Tornador, Laia Bassaganyas, et al.
Bone
|
May 27, 2022
Clinical description and genetic analysis of a novel familial skeletal dysplasia characterized by high bone mass and lucent bone lesions
Diana Ovejero, Natalia Garcia-Giralt, Núria Martínez-Gil, et al.
Journal of Medical Genetics
|
March 28, 2024
Subcellular localisation of truncated MAGEL2 proteins: insight into the molecular pathology of Schaaf-Yang syndrome
Mónica Centeno-Pla, Estefanía Alcaide-Consuegra, Sophie Gibson, et al.
Journal of Affective Disorders
|
February 18, 2020
Exploring genetic variants in obsessive compulsive disorder severity: A GWAS approach
María Alemany-Navarro, Raquel Cruz, Eva Real, et al.
Genes
|
January 21, 2022
Gene Network of Susceptibility to Atypical Femoral Fractures Related to Bisphosphonate Treatment
Natalia Garcia-Giralt, Neus Roca-Ayats, Josep F Abril, et al.
Pain
|
March 4, 2014
Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system
Elisa Docampo, Georgia Escaramís, Mònica Gratacòs, et al.
International Journal of Molecular Sciences
|
July 24, 2021
Functional Analyses of Four <i>CYP1A1</i> Missense Mutations Present in Patients with Atypical Femoral Fractures
Nerea Ugartondo, Núria Martínez-Gil, Mònica Esteve, et al.
International Journal of Molecular Sciences
|
February 9, 2021
<i>De Novo PORCN</i> and <i>ZIC2</i> Mutations in a Highly Consanguineous Family
Laura Castilla-Vallmanya, Semra Gürsoy, Özlem Giray-Bozkaya, et al.
Biochimica Et Biophysica Acta
|
November 26, 2008
Are MYO1C and MYO1F associated with hearing loss?
Cristina Zadro, Maria Stella Alemanno, Emanuele Bellacchio, et al.
Arthritis and Rheumatism
|
March 10, 2010
Deletion of the late cornified envelope genes, LCE3C and LCE3B, is associated with rheumatoid arthritis
Elisa Docampo, Raquel Rabionet, Eva Riveira-Muñoz, et al.
Page
of 7