Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with Costello syndrome.

Authors :: Maróti Z
Kutsche K
Sutajova M
Gal A
Nothwang HG
Czeizel AE
Tímár L
Sólyom E
Source :: American journal of medical genetics [Am J Med Genet] 2002 May 01; Vol. 109 (3), pp. 234-7.
Publication Year :: 2002

Subjects :: Abnormalities, Multiple pathology
Cardiomyopathies pathology
Face abnormalities
Humans
In Situ Hybridization, Fluorescence
Intellectual Disability pathology
Skin Abnormalities pathology
Syndrome
Abnormalities, Multiple genetics
Chromosome Breakage
Chromosomes, Human, Pair 1 genetics
Chromosomes, Human, Pair 22 genetics
Growth Disorders pathology
Translocation, Genetic

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