Ring chromosome 14 mosaicism: An unusual case associated with developmental delay and epilepsy, characterized by genome array-CGH

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Bibliographic Details
Published inAmerican journal of medical genetics. Part A Vol. 152A; no. 1; pp. 234 - 236
Main Authors Nucaro, Anna Lisa, Falchi, Melania, Pisano, Tiziana, Rossino, Rossano, Boscarelli, Francesca, Stoico, Giusi, Milia, Angela, Montaldo, Caterina, Cianchetti, Carlo, Pruna, Dario
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.01.2010
Wiley-Liss
Subjects
Biological and medical sciences
Chromosomes, Human, Pair 14
Developmental Disabilities - genetics
Epilepsy - genetics
Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
Humans
In Situ Hybridization, Fluorescence
Infant
Karyotyping
Medical genetics
Medical sciences
Nervous system (semeiology, syndromes)
Neurology
Nucleic Acid Hybridization
Ring Chromosomes
Chromosomal aberration
Case study
Nervous system diseases
Ring chromosome
Epilepsy
Central nervous system disease
Abnormal chromosome
Chromosome D14
Mosaicism
Developmental disorder
Genome
Cerebral disorder
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Bibliography:How to Cite this Article: Nucaro AL, Falchi M, Pisano T, Rossino R, Boscarelli F, Stoico G, Milia A, Montaldo C, Cianchetti C, Pruna D. 2010. Ring chromosome 14 mosaicism: An unusual case associated with developmental delay and epilepsy, characterized by genome array-CGH. Am J Med Genet Part A 152A:234-236.
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ArticleID:AJMG33167
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How to Cite this Article: Nucaro AL, Falchi M, Pisano T, Rossino R, Boscarelli F, Stoico G, Milia A, Montaldo C, Cianchetti C, Pruna D. 2010. Ring chromosome 14 mosaicism: An unusual case associated with developmental delay and epilepsy, characterized by genome array‐CGH. Am J Med Genet Part A 152A:234–236.
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.33167