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Familial pericentric inversion of chromosome 12.
Voiculescu I, Barbi G, Wolff G, Steinbach P, Back E, Schempp W. Voiculescu I, et al. Among authors: schempp w. Hum Genet. 1986 Apr;72(4):320-2. doi: 10.1007/BF00290957. Hum Genet. 1986. PMID: 3699821
Trisomy 22 in a newborn with multiple malformations.
Voiculescu I, Back E, Duncan AM, Schwaibold H, Schempp W. Voiculescu I, et al. Among authors: schempp w. Hum Genet. 1987 Jul;76(3):298-301. doi: 10.1007/BF00283629. Hum Genet. 1987. PMID: 3474207
An excess of chromosome 1 breakpoints in male infertility.
Bache I, Assche EV, Cingoz S, Bugge M, Tümer Z, Hjorth M, Lundsteen C, Lespinasse J, Winther K, Niebuhr A, Kalscheuer V, Liebaers I, Bonduelle M, Tournaye H, Ayuso C, Barbi G, Blennow E, Bourrouillou G, Brondum-Nielsen K, Bruun-Petersen G, Croquette MF, Dahoun S, Dallapiccola B, Davison V, Delobel B, Duba HC, Duprez L, Ferguson-Smith M, Fitzpatrick DR, Grace E, Hansmann I, Hultén M, Jensen PK, Jonveaux P, Kristoffersson U, Lopez-Pajares I, McGowan-Jordan J, Murken J, Orera M, Parkin T, Passarge E, Ramos C, Rasmussen K, Schempp W, Schubert R, Schwinger E, Shabtai F, Smith K, Stallings R, Stefanova M, Tranebjerg L, Turleau C, van der Hagen CB, Vekemans M, Vokac NK, Wagner K, Wahlstroem J, Zelante L, Tommerup N. Bache I, et al. Among authors: schempp w. Eur J Hum Genet. 2004 Dec;12(12):993-1000. doi: 10.1038/sj.ejhg.5201263. Eur J Hum Genet. 2004. PMID: 15367911
130 results