Luis Becerra-Solano

Luis Becerra-Solano

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Luis Becerra-Solano

Luis Becerra-Solano

Publications by authors named "Luis Becerra-Solano"

11Publications

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1PubMed Central Citations

PEDIA: prioritization of exome data by image analysis.

Genet Med 2019 Jun 5. Epub 2019 Jun 5.

Institute of Genomic Statistics and Bioinformatics, University of Bonn, Bonn, Germany.

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http://dx.doi.org/10.1038/s41436-019-0566-2DOI Listing
June 2019

Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder.

J Autism Dev Disord 2019 Mar 2. Epub 2019 Mar 2.

Departamento de Bioquímica y Medicina Molecular, Facultad de Medicina, Universidad Autónoma de Nuevo León, Av. Fco. I. Madero s/n, Mitras Centro, Monterrey, Nuevo León, Mexico.

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http://dx.doi.org/10.1007/s10803-019-03951-zDOI Listing
March 2019

An update on amniotic bands sequence.

Arch Argent Pediatr 2018 06;116(3):e409-e420

Unidad de Investigación Médica en Medicina Reproductiva, Unidad Médica de Alta Especialidad, Hospital de Ginecoobstetricia Nº 4 Luis Castelazo Ayala, Instituto Mexicano del Seguro Social, Ciudad de México.

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http://www.sap.org.ar/docs/publicaciones/archivosarg/2018/v1
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http://dx.doi.org/10.5546/aap.2018.eng.e409DOI Listing
June 2018

Uncommon runs of homozygosity disclose homozygous missense mutations in two ciliopathy-related genes (SPAG17 and WDR35) in a patient with multiple brain and skeletal anomalies.

Eur J Med Genet 2018 Mar 23;61(3):161-167. Epub 2017 Nov 23.

División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, 44340, Guadalajara, Jalisco, Mexico; Dirección de Educación e Investigación en Salud, UMAE Hospital de Gineco-Obstretricia, CMNO-IMSS, 44340, Guadalajara, Jalisco, Mexico. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2017.11.011DOI Listing
March 2018

Severe Craniofacial Involvement due to Amniotic Band Sequence.

Fetal Pediatr Pathol 2018 Feb 16;37(1):27-37. Epub 2018 Jan 16.

i Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, División de Genética , Sierra Mojada 800, Guadalajara , Mexico.

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https://www.tandfonline.com/doi/full/10.1080/15513815.2017.1
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http://dx.doi.org/10.1080/15513815.2017.1392663DOI Listing
February 2018

Bosma arrhinia microphthalmia syndrome in a Mexican patient with a molecular analysis of PAX6.

Clin Dysmorphol 2016 Jan;25(1):12-5

aGenetics Division, Western Biomedical Research Center, CMNO-IMSS, Guadalajara, Jalisco bTeleton Children's Rehabilitation Center, Chihuahua, Chihuahua cResearch Unit, Institute of Ophthalmology, Conde de Valenciana Foundation, Mexico City, Mexico.

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http://dx.doi.org/10.1097/MCD.0000000000000101DOI Listing
January 2016

Expanding the phenotype of spondylospinal thoracic dysostosis (the Turkel-Chen-Johnson syndrome).

Clin Dysmorphol 2015 Jan;24(1):1-6

aChildren's Rehabilitation Center Teleton, Chihuahua City, Chihuahua bDivision of Genetics, Western Biomedical Research Center, IMSS, Guadalajara, Jalisco, Mexico.

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http://dx.doi.org/10.1097/MCD.0000000000000058DOI Listing
January 2015

[True hermaphroditism and sequences. Diagnostic implications regarding two cases].

Rev Med Inst Mex Seguro Soc 2008 Sep-Oct;46(5):539-42

Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara.

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April 2009

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

Clin Dysmorphol 2008 Jan;17(1):27-30

División de Genética, Centro de Investigación Biomédica de Occidente-Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, México.

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http://dx.doi.org/10.1097/MCD.0b013e3282ef947dDOI Listing
January 2008

A 9p13-->p24 duplication coupled with a whole 22q translocation onto 9p24.

J Appl Genet 2007 ;48(1):95-8

Centro de Investigación Biomédica de Occidente, IMSS, Ap. Postal 1-3838, Guadalajara, Jal., Mexico.

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March 2007