Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome.

Tadin-Strapps, M; Warburton, D; Baumeister, F A M; Fischer, S G; Yonan, J; Gilliam, T C; Christiano, A M

Tadin-Strapps, M; Warburton, D; Baumeister, F A M; Fischer, S G; Yonan, J; Gilliam, T C; Christiano, A M.

Affiliation

Tadin-Strapps M; Department ofDermatology, Columbia University, New York, NY 10032, USA.

Cytogenet Genome Res ; 107(1-2): 68-76, 2004.

Article in En | MEDLINE | ID: mdl-15305058

Subject(s)

Abnormalities, Multiple/genetics; Chromosome Breakage/genetics; Chromosome Inversion/genetics; Chromosomes, Human, Pair 8/genetics; Cloning, Molecular/methods; Facial Asymmetry/genetics; Hypertrichosis/genetics; Tooth Abnormalities/genetics; Female; Humans; Infant, Newborn; Syndrome

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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Tooth Abnormalities / Abnormalities, Multiple / Chromosomes, Human, Pair 8 / Cloning, Molecular / Chromosome Breakage / Facial Asymmetry / Hypertrichosis / Chromosome Inversion Limits: Female / Humans / Newborn Language: En Journal: Cytogenet Genome Res Year: 2004 Document type: Article

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