A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.

Courtens, Winnie; Wuyts, Wim; Scheers, Stefaan; Van Luijk, Rob; Reyniers, Edwin; Rooms, Liesbeth; Ceulemans, Berten; Kooy, Frank; Wauters, Jan

Courtens, Winnie; Wuyts, Wim; Scheers, Stefaan; Van Luijk, Rob; Reyniers, Edwin; Rooms, Liesbeth; Ceulemans, Berten; Kooy, Frank; Wauters, Jan.

Affiliation

Courtens W; Department of Medical Genetics, University Hospital Antwerp, Antwerp, Belgium. winnie.courtens@ua.ac.be

Eur J Med Genet ; 49(5): 402-13, 2006.

Article in En | MEDLINE | ID: mdl-16488200

Subject(s)

Abnormalities, Multiple/genetics; Aneuploidy; Chromosome Deletion; Chromosomes, Human, Pair 10/genetics; Chromosomes, Human, Pair 18/genetics; Intellectual Disability/genetics; Child, Preschool; Female; Humans; In Situ Hybridization, Fluorescence; Microsatellite Repeats; Nucleic Acid Amplification Techniques; Translocation, Genetic; Trisomy

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Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 10 / Chromosomes, Human, Pair 18 / Chromosome Deletion / Aneuploidy / Intellectual Disability Limits: Child, preschool / Female / Humans Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2006 Type: Article Affiliation country: Belgium

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