An intellectually disabled patient with the 5q14.3q15 microdeletion syndrome associated with an apparently de novo t(2;5)(q13;q14)

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Bibliographic Details
Published inAmerican journal of medical genetics. Part A Vol. 158A; no. 4; pp. 942 - 946
Main Authors Toral-López, Jaime, Buentello-Volante, Beatriz, Balderas-Minor, Marta M., Amezcua-Herrera, Carmen, Valdes-Miranda, Juan M., González-Huerta, Luz Ma, Gudiño, Marco, Cuevas-Covarrubias, Sergio A., Zenteno, Juan Carlos
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.04.2012
Wiley-Liss
Wiley Subscription Services, Inc
Subjects
Abnormalities, Multiple - genetics
Adult and adolescent clinical studies
Biological and medical sciences
Child, Preschool
Chromosome aberrations
Chromosome Deletion
Chromosomes, Human, Pair 2 - genetics
Chromosomes, Human, Pair 5 - genetics
Female
Humans
In Situ Hybridization, Fluorescence
Intellectual deficiency
Intellectual Disability - genetics
MADS Domain Proteins - genetics
Medical genetics
Medical sciences
MEF2 Transcription Factors
Myogenic Regulatory Factors - genetics
Oligonucleotide Array Sequence Analysis
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Translocation, Genetic
Chromosomal aberration
Human
Microdeletion
Intellectual deficiency
Abnormal chromosome
Patient
Developmental disorder
Mental retardation
De novo
Chromosome translocation
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Bibliography:How to Cite this Article: Toral-López J, Buentello-Volante B, Balderas-Minor MM, Amezcua-Herrera C, Valdes-Miranda JM, González-Huerta LM, Gudiño M, Cuevas-Covarrubias SA, Zenteno JC. 2012. An intellectually disabled patient with the 5q14.3q15 microdeletion syndrome associated with an apparently de novo t(2;5)(q13;q14). Am J Med Genet Part A 158A:942-946.
ArticleID:AJMG35262
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How to Cite this Article: Toral‐López J, Buentello‐Volante B, Balderas‐Minor MM, Amezcua‐Herrera C, Valdes‐Miranda JM, González‐Huerta LM, Gudiño M, Cuevas‐Covarrubias SA, Zenteno JC. 2012. An intellectually disabled patient with the 5q14.3q15 microdeletion syndrome associated with an apparently de novo t(2;5)(q13;q14). Am J Med Genet Part A 158A:942–946.
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ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.35262