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Del(18)(q12.2q21.1) caused by a paternal sister chromatid rearrangement in a developmentally delayed girlKOTZOT, Dieter; HABERLANDT, Edda; FAUTH, Christine et al.American journal of medical genetics. 2005, Vol 135A, Num 3, pp 304-307, issn 0148-7299, 4 p.Article

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Molecular Characterization of a de novo Ring Chromosome 6 in a Growth Retarded but Otherwise Healthy WomanHÖCKNER, Martina; UTERMANN, Barbara; ERDEL, Martin et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 7, pp 925-929, issn 1552-4825, 5 p.Article

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Rare Interstitial Deletion 9q31.2 to q33.1 de novo : Longitudinal Study in a Patient Over a Period of More Than 20 YearsGAMERDINGER, Ulrike; EGGERMANN, Thomas; SCHUBERT, Regine et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 9, pp 1180-1184, issn 1552-4825, 5 p.Article

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L''empreinte génomique parentale = Parental genomic imprintingBABINET, C.Annales de génétique (Paris). 1993, Vol 36, Num 1, pp 63-69, issn 0003-3995Conference Paper