Towards mapping phenotypical traits in 18p− syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation

Author:

Brenk Christian H,Prott Eva-Christina,Trost Detlef,Hoischen Alexander,Walldorf Constanze,Radlwimmer Bernhard,Wieczorek Dagmar,Propping Peter,Gillessen-Kaesbach Gabriele,Weber Ruthild G,Engels Hartmut

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference34 articles.

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2. Schinzel A : Catalogue of unbalanced chromosome aberrations in man. Berlin: Walter de Gruyter, 2001.

3. Rigola MA, Plaja A, Mediano C, Miro R, Egozcue J, Fuster C : Characterization of a heritable partial monosomy 18p by molecular and cytogenetic analysis. Am J Med Genet 2001; 104: 37–41.

4. Schaub RL, Reveles XT, Baillargeon J, Leach RJ, Cody JD : Molecular characterization of 18p deletions: evidence for a breakpoint cluster. Genet Med 2002; 4: 15–19.

5. Lurie IW, Lazjuk GI : Partial monosomies 18. Review of cytogenetical and phenotypical variants. Humangenetik 1972; 15: 203–222.

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