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FMR1, FMR2, and SLITRK2 deletion inside a paracentric inversion involving bands Xq27.3-q28 in a male and his mother

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Bibliographic Details
Published in:	American journal of medical genetics. Part A 2011-01, Vol.155A (1), p.221-224
Main Authors:	Cavani, Simona, Prontera, Paolo, Grasso, Marina, Ardisia, Carmela, Malacarne, Michela, Gradassi, Cristina, Cecconi, Massimiliano, Mencarelli, Amedea, Donti, Emilio, Pierluigi, Mauro
Format:	Article
Language:	English
Subjects:	Adolescent Adult Biological and medical sciences Chromosome Deletion Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...) Chromosome Inversion Chromosomes, Human, X - genetics Comparative Genomic Hybridization Female Fragile X Mental Retardation Protein - genetics Fragile X Syndrome - genetics Fragile X Syndrome - pathology Humans In Situ Hybridization, Fluorescence Male Medical genetics Medical sciences Membrane Proteins - genetics Nuclear Proteins - genetics
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