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Page 1
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: zelante l. Eur J Hum Genet. 2004 Dec;12(12):993-1000. doi: 10.1038/sj.ejhg.5201263. Eur J Hum Genet. 2004. PMID: 15367911
The 18ph+ chromosome heteromorphism.
Zelante L, Notarangelo A, Dallapiccola B. Zelante L, et al. Prenat Diagn. 1994 Nov;14(11):1096-7. doi: 10.1002/pd.1970141119. Prenat Diagn. 1994. PMID: 7877960 No abstract available.
Umbilical cord pseudocyst in trisomy 13.
Zelante L, Dallapiccola B. Zelante L, et al. Prenat Diagn. 1989 Jun;9(6):448-9. doi: 10.1002/pd.1970090615. Prenat Diagn. 1989. PMID: 2668919 No abstract available.
Isodicentric Xq in Klinefelter syndrome.
Zelante L, Calvano S, Dallapiccola B. Zelante L, et al. Am J Med Genet. 1991 Nov 1;41(2):267-8. doi: 10.1002/ajmg.1320410229. Am J Med Genet. 1991. PMID: 1785649 Review. No abstract available.
Two mosaic-YY males carrying asymmetric Y chromosomes.
Zelante L, Dallapiccola B, Calvano S, Memeo E, Gasparini P, Simi P, Rossi S, Finelli P, Rocchi M, Archidiacono N. Zelante L, et al. Clin Genet. 1997 Jan;51(1):65-8. doi: 10.1111/j.1399-0004.1997.tb02418.x. Clin Genet. 1997. PMID: 9084939
242 results