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Neuroscience|January 6, 2009

Brain-derived neurotrophic factor modulates the severity of cognitive alterations induced by mutant huntingtin: involvement of phospholipaseCgamma activity and glutamate receptor expressionA Giralt, T Rodrigo, E D Martín, et al.

Clinical Genetics|April 23, 2016

Social anxiety and autism spectrum traits among adult FMR1 premutation carriersO López-Mourelo, E Mur, I Madrigal, et al.

Reproductive Biomedicine Online|August 31, 2010

Fragile X syndrome prenatal diagnosis: parental attitudes and reproductive responsesM Xunclà, C Badenas, M Domínguez, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 17, 2007

MLPA as first screening method for the detection of microduplications and microdeletions in patients with X-linked mental retardationIrene Madrigal, Laia Rodríguez-Revenga, Celia Badenas, et al.

Journal of Molecular Medicine (Berlin, Germany)|July 4, 2001

Large de novo deletion in chromosome 12 affecting the PAH, IGF1, ASCL1, and TRA1 genesJ Mallolas, M A Vilaseca, C Pavia, et al.

Anales Espanoles De Pediatria|March 1, 1996

[A genetic and molecular study of 85 families affected with the fragile X syndrome]M Milà Recasens, A Sánchez Díaz, G Glover López, et al.

Lancet (London, England)|March 3, 1998

Connexin-26 mutations in sporadic and inherited sensorineural deafnessX Estivill, P Fortina, S Surrey, et al.

Genes, Brain, and Behavior|June 25, 2013

MicroRNA expression profiling in blood from fragile X-associated tremor/ataxia syndrome patientsM I Alvarez-Mora, L Rodriguez-Revenga, I Madrigal, et al.

Radiologia|March 14, 2009

[Comparative study of sentinel node biopsy in patients with multifocal breast carcinoma versus in those with unifocal breast carcinoma.]M Solá, M Fraile, A Mariscal, et al.

BMC Genomics|December 1, 2007

X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardationI Madrigal, L Rodríguez-Revenga, L Armengol, et al.

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Showing results (51-60 of 63) with videos related to

Sort By:

Pageof 7

Neuroscience|January 6, 2009

Brain-derived neurotrophic factor modulates the severity of cognitive alterations induced by mutant huntingtin: involvement of phospholipaseCgamma activity and glutamate receptor expressionA Giralt, T Rodrigo, E D Martín, et al.

Clinical Genetics|April 23, 2016

Social anxiety and autism spectrum traits among adult FMR1 premutation carriersO López-Mourelo, E Mur, I Madrigal, et al.

Reproductive Biomedicine Online|August 31, 2010

Fragile X syndrome prenatal diagnosis: parental attitudes and reproductive responsesM Xunclà, C Badenas, M Domínguez, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 17, 2007

MLPA as first screening method for the detection of microduplications and microdeletions in patients with X-linked mental retardationIrene Madrigal, Laia Rodríguez-Revenga, Celia Badenas, et al.

Journal of Molecular Medicine (Berlin, Germany)|July 4, 2001

Large de novo deletion in chromosome 12 affecting the PAH, IGF1, ASCL1, and TRA1 genesJ Mallolas, M A Vilaseca, C Pavia, et al.

Anales Espanoles De Pediatria|March 1, 1996

[A genetic and molecular study of 85 families affected with the fragile X syndrome]M Milà Recasens, A Sánchez Díaz, G Glover López, et al.

Lancet (London, England)|March 3, 1998

Connexin-26 mutations in sporadic and inherited sensorineural deafnessX Estivill, P Fortina, S Surrey, et al.

Genes, Brain, and Behavior|June 25, 2013

MicroRNA expression profiling in blood from fragile X-associated tremor/ataxia syndrome patientsM I Alvarez-Mora, L Rodriguez-Revenga, I Madrigal, et al.

Radiologia|March 14, 2009

[Comparative study of sentinel node biopsy in patients with multifocal breast carcinoma versus in those with unifocal breast carcinoma.]M Solá, M Fraile, A Mariscal, et al.

BMC Genomics|December 1, 2007

X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardationI Madrigal, L Rodríguez-Revenga, L Armengol, et al.

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