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

Maróti, Zoltán; Kutsche, Kerstin; Sutajova, Marketa; Gal, Andreas; Nothwang, Hans Gerd; Czeizel, Andrew E; Tímár, László; Sólyom, Enikö

Maróti, Zoltán; Kutsche, Kerstin; Sutajova, Marketa; Gal, Andreas; Nothwang, Hans Gerd; Czeizel, Andrew E; Tímár, László; Sólyom, Enikö.

Am J Med Genet ; 109(3): 234-7, 2002 May 01.

Article in En | MEDLINE | ID: mdl-11977185

Subject(s)

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

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Collection: 01-internacional Database: MEDLINE Main subject: Translocation, Genetic / Abnormalities, Multiple / Chromosomes, Human, Pair 1 / Chromosomes, Human, Pair 22 / Chromosome Breakage / Growth Disorders Limits: Humans Language: En Journal: Am J Med Genet Year: 2002 Document type: Article Country of publication: United States

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