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

Authors :: Marina Grasso
Paolo Prontera
Amedea Mencarelli
Mauro Pierluigi
Emilio Donti
Simona Cavani
Michela Malacarne
Cristina Gradassi
Carmela Ardisia
Massimiliano Cecconi
Source :: American Journal of Medical Genetics Part A. 155:221-224
Publication Year :: 2010
Publisher :: Wiley, 2010.

Subjects :: Adult
Male
Genetics
Chromosomes, Human, X
Comparative Genomic Hybridization
Adolescent
Membrane Proteins
Nuclear Proteins
Biology
FMR1
Fragile X Mental Retardation Protein
Fragile X Syndrome
Chromosome Inversion
Humans
Female
Chromosome Deletion
In Situ Hybridization, Fluorescence
Genetics (clinical)
Chromosomal inversion

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