Lundsteen C - Search Results

1

Interstitial deletion of the short arm of chromosome 1: attempt to establish a clinical phenotype (46,XX,del (1)(p22p32)).

Mircher C, Rethore MO, Lespinasse J, Fert-Ferrer S, Lundsteen C, Kirchoff M. Mircher C, et al. Among authors: lundsteen c. Am J Med Genet A. 2003 Apr 15;118A(2):176-9. doi: 10.1002/ajmg.a.10052. Am J Med Genet A. 2003. PMID: 12655498 Review.

2

De novo complex chromosomal rearrangements (CCR) involving chromosome 1, 5, and 6 resulting in microdeletion for 6q14 in a female carrier with psychotic disorder.

Lespinasse J, Bugge M, Réthoré MO, North MO, Lundsteen C, Kirchhoff M. Lespinasse J, et al. Among authors: lundsteen c. Am J Med Genet A. 2004 Jul 15;128A(2):199-203. doi: 10.1002/ajmg.a.30064. Am J Med Genet A. 2004. PMID: 15214017

3

Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases.

Lespinasse J, Réthoré MO, North MO, Bovier-Lapierre M, Lundsteen C, Fert-Ferrer S, Bugge M, Kirchoff M. Lespinasse J, et al. Among authors: lundsteen c. Ann Genet. 2004 Jul-Sep;47(3):315-24. doi: 10.1016/j.anngen.2004.05.002. Ann Genet. 2004. PMID: 15337478

4

Non-disjunction of chromosome 13.

Bugge M, Collins A, Hertz JM, Eiberg H, Lundsteen C, Brandt CA, Bak M, Hansen C, Delozier CD, Lespinasse J, Tranebjaerg L, Hahnemann JM, Rasmussen K, Bruun-Petersen G, Duprez L, Tommerup N, Petersen MB. Bugge M, et al. Among authors: lundsteen c. Hum Mol Genet. 2007 Aug 15;16(16):2004-10. doi: 10.1093/hmg/ddm148. Epub 2007 Jun 21. Hum Mol Genet. 2007. PMID: 17584770

5

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: lundsteen c. Eur J Hum Genet. 2004 Dec;12(12):993-1000. doi: 10.1038/sj.ejhg.5201263. Eur J Hum Genet. 2004. PMID: 15367911

6

High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes.

Kirchhoff M, Rose H, Maahr J, Gerdes T, Bugge M, Tommerup N, Tümer Z, Lespinasse J, Jensen PK, Wirth J, Lundsteen C. Kirchhoff M, et al. Among authors: lundsteen c. Eur J Hum Genet. 2000 Sep;8(9):661-8. doi: 10.1038/sj.ejhg.5200512. Eur J Hum Genet. 2000. PMID: 10980571

7

Interstitial deletion in the "critical region" of the long arm of the X chromosome in a mentally retarded boy and his normal mother.

Tabor A, Andersen O, Lundsteen C, Niebuhr E, Sardemann H. Tabor A, et al. Among authors: lundsteen c. Hum Genet. 1983;64(2):196-9. doi: 10.1007/BF00327127. Hum Genet. 1983. PMID: 6885061

8

Choroideremia in interstitial deletion of the X chromosome.

Rosenberg T, Schwartz M, Niebuhr E, Yang HM, Sardemann H, Andersen O, Lundsteen C. Rosenberg T, et al. Among authors: lundsteen c. Ophthalmic Paediatr Genet. 1986 Dec;7(3):205-10. doi: 10.3109/13816818609004140. Ophthalmic Paediatr Genet. 1986. PMID: 2882458

9

Further delineation of the 22q13 deletion syndrome.

Lindquist SG, Kirchhoff M, Lundsteen C, Pedersen W, Erichsen G, Kristensen K, Lillquist K, Smedegaard HH, Skov L, Tommerup N, Brøndum-Nielsen K. Lindquist SG, et al. Among authors: lundsteen c. Clin Dysmorphol. 2005 Apr;14(2):55-60. Clin Dysmorphol. 2005. PMID: 15770125

10

High resolution comparative genomic hybridisation in clinical cytogenetics.

Kirchhoff M, Rose H, Lundsteen C. Kirchhoff M, et al. Among authors: lundsteen c. J Med Genet. 2001 Nov;38(11):740-4. doi: 10.1136/jmg.38.11.740. J Med Genet. 2001. PMID: 11694545 Free PMC article.

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