Early detection of chromosome 9q22.32q31.1 microdeletion and the nevoid basal cell carcinoma syndrome.

de Ravel, Thomy J L; Ameye, Liliane; Ballon, Katleen; Borghgraef, Martine; Vermeesch, Joris R; Devriendt, Koen

de Ravel, Thomy J L; Ameye, Liliane; Ballon, Katleen; Borghgraef, Martine; Vermeesch, Joris R; Devriendt, Koen.

Affiliation

de Ravel TJ; Centre for Human Genetics, UZ Leuven, Herestraat 49, 3000 Leuven, Belgium. thomy.deravel@uzleuven.be

Eur J Med Genet ; 52(2-3): 145-7, 2009.

Article in En | MEDLINE | ID: mdl-19233320

Subject(s)

Chromosome Deletion; Chromosome Disorders/genetics; Chromosomes, Human, Pair 9; Abnormalities, Multiple/genetics; Carcinoma, Basal Cell/genetics; Humans; Infant; Intellectual Disability; Male; Motor Skills Disorders; Patched Receptors; Patched-1 Receptor; Receptors, Cell Surface/genetics; Speech Disorders; Syndrome

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Full text: 1 Database: MEDLINE Main subject: Chromosomes, Human, Pair 9 / Chromosome Deletion / Chromosome Disorders Type of study: Diagnostic_studies / Screening_studies Limits: Humans / Infant / Male Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2009 Type: Article Affiliation country: Belgium

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