Similar articles for PMID: 12960216

Year	Number of Results
1983	1
1985	1
1986	1
1989	1
1990	1
1992	2
1993	3
1995	3
1996	3
1997	2
1998	4
1999	2
2000	5
2001	3
2002	5
2003	9
2004	7
2005	9
2006	3
2007	6
2009	1
2010	4
2011	8
2012	4
2013	6
2016	2
2019	1
2021	1
2024	0

1

Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations.

Luciani JJ, de Mas P, Depetris D, Mignon-Ravix C, Bottani A, Prieur M, Jonveaux P, Philippe A, Bourrouillou G, de Martinville B, Delobel B, Vallee L, Croquette MF, Mattei MG. Luciani JJ, et al. J Med Genet. 2003 Sep;40(9):690-6. doi: 10.1136/jmg.40.9.690. J Med Genet. 2003. PMID: 12960216 Free PMC article. No abstract available.

2

Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome.

Bonaglia MC, Giorda R, Beri S, De Agostini C, Novara F, Fichera M, Grillo L, Galesi O, Vetro A, Ciccone R, Bonati MT, Giglio S, Guerrini R, Osimani S, Marelli S, Zucca C, Grasso R, Borgatti R, Mani E, Motta C, Molteni M, Romano C, Greco D, Reitano S, Baroncini A, Lapi E, Cecconi A, Arrigo G, Patricelli MG, Pantaleoni C, D'Arrigo S, Riva D, Sciacca F, Dalla Bernardina B, Zoccante L, Darra F, Termine C, Maserati E, Bigoni S, Priolo E, Bottani A, Gimelli S, Bena F, Brusco A, di Gregorio E, Bagnasco I, Giussani U, Nitsch L, Politi P, Martinez-Frias ML, Martínez-Fernández ML, Martínez Guardia N, Bremer A, Anderlid BM, Zuffardi O. Bonaglia MC, et al. PLoS Genet. 2011 Jul;7(7):e1002173. doi: 10.1371/journal.pgen.1002173. Epub 2011 Jul 14. PLoS Genet. 2011. PMID: 21779178 Free PMC article.

3

Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.

Ballif BC, Wakui K, Gajecka M, Shaffer LG. Ballif BC, et al. Hum Genet. 2004 Jan;114(2):198-206. doi: 10.1007/s00439-003-1029-y. Epub 2003 Oct 25. Hum Genet. 2004. PMID: 14579147

4

Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4--KCNQ2 genes loci.

Elghezal H, Hannachi H, Mougou S, Kammoun H, Triki C, Saad A. Elghezal H, et al. Eur J Med Genet. 2007 Nov-Dec;50(6):441-5. doi: 10.1016/j.ejmg.2007.07.002. Epub 2007 Aug 6. Eur J Med Genet. 2007. PMID: 17851150

5

[Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].

Esmer MC, Carnevale A, Gómez L, del Castillo V, Frías S. Esmer MC, et al. Rev Invest Clin. 1996 Jan-Feb;48(1):27-33. Rev Invest Clin. 1996. PMID: 8815483 Spanish.

6

Cryptic subtelomeric translocations in the 22q13 deletion syndrome.

Praphanphoj V, Goodman BK, Thomas GH, Raymond GV. Praphanphoj V, et al. J Med Genet. 2000 Jan;37(1):58-61. doi: 10.1136/jmg.37.1.58. J Med Genet. 2000. PMID: 10633138 Free PMC article.

7

Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.

Plotner PL, Smith JL, Northrup H. Plotner PL, et al. Am J Med Genet. 2002 Jul 22;111(1):71-5. doi: 10.1002/ajmg.10420. Am J Med Genet. 2002. PMID: 12124739 Review.

8

[Terminal 1q deletion by translocation t(1;20)pat, confirmed by in situ hybridization].

López-Ginés C, Gil-Benso R, Gregori-Romero MA, Paredes-Cencillo C, Castelló-Pomares M, Llombart-Bosch A. López-Ginés C, et al. An Esp Pediatr. 1998 Mar;48(3):309-11. An Esp Pediatr. 1998. PMID: 9608096 Spanish. No abstract available.

9

A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18.

Safavi M, Haghi Ashtiani MT, Badv RS, Azari-Yam A, Vasei M. Safavi M, et al. Arch Iran Med. 2019 Oct 1;22(10):627-628. Arch Iran Med. 2019. PMID: 31679365

10

FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes.

Ballif BC, Kashork CD, Shaffer LG. Ballif BC, et al. Eur J Hum Genet. 2000 Oct;8(10):764-70. doi: 10.1038/sj.ejhg.5200536. Eur J Hum Genet. 2000. PMID: 11039576

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

89 results

Results by year