Similar articles for PMID: 8102569

Year	Number of Results
1987	1
1988	1
1989	2
1990	2
1991	4
1992	5
1993	13
1994	8
1995	2
1996	3
1997	2
1999	4
2000	1
2001	3
2003	4
2005	2
2007	1
2010	1
2012	2
2024	0

1

A disease-associated germline deletion maps the type 2 neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukaemia inhibitory factor locus.

Watson CJ, Gaunt L, Evans G, Patel K, Harris R, Strachan T. Watson CJ, et al. Hum Mol Genet. 1993 Jun;2(6):701-4. doi: 10.1093/hmg/2.6.701. Hum Mol Genet. 1993. PMID: 8102569

2

A t(17;22)(q21;q12) with partial ETV4 deletion in a soft tissue Ewing sarcoma.

Rougemont AL, Bouron-Dal Soglio D, Patey-Mariaud de Serre N, Fetni R, Fan L, Barrette S, Fournet JC. Rougemont AL, et al. Cancer Genet. 2012 Jan-Feb;205(1-2):55-60. doi: 10.1016/j.cancergen.2012.01.007. Cancer Genet. 2012. PMID: 22429598

3

Ring chromosome 22 and neurofibromatosis type II: proof of two-hit model for the loss of the NF2 gene in the development of meningioma.

Zirn B, Arning L, Bartels I, Shoukier M, Hoffjan S, Neubauer B, Hahn A. Zirn B, et al. Clin Genet. 2012 Jan;81(1):82-7. doi: 10.1111/j.1399-0004.2010.01598.x. Epub 2010 Dec 22. Clin Genet. 2012. PMID: 21175598

4

Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus.

Hansson CM, Buckley PG, Grigelioniene G, Piotrowski A, Hellström AR, Mantripragada K, Jarbo C, Mathiesen T, Dumanski JP. Hansson CM, et al. BMC Genomics. 2007 Jan 12;8:16. doi: 10.1186/1471-2164-8-16. BMC Genomics. 2007. PMID: 17222329 Free PMC article.

5

Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2.

Buckley PG, Mantripragada KK, Díaz de Ståhl T, Piotrowski A, Hansson CM, Kiss H, Vetrie D, Ernberg IT, Nordenskjöld M, Bolund L, Sainio M, Rouleau GA, Niimura M, Wallace AJ, Evans DG, Grigelionis G, Menzel U, Dumanski JP. Buckley PG, et al. Hum Mutat. 2005 Dec;26(6):540-9. doi: 10.1002/humu.20255. Hum Mutat. 2005. PMID: 16287142

6

Sensitive detection of deletions of one or more exons in the neurofibromatosis type 2 (NF2) gene by multiplexed gene dosage polymerase chain reaction.

Diebold R, Bartelt-Kirbach B, Evans DG, Kaufmann D, Hanemann CO. Diebold R, et al. J Mol Diagn. 2005 Feb;7(1):97-104. doi: 10.1016/S1525-1578(10)60014-1. J Mol Diagn. 2005. PMID: 15681480 Free PMC article.

7

Somatic instability of the NF2 gene in schwannomatosis.

Kaufman DL, Heinrich BS, Willett C, Perry A, Finseth F, Sobel RA, MacCollin M. Kaufman DL, et al. Arch Neurol. 2003 Sep;60(9):1317-20. doi: 10.1001/archneur.60.9.1317. Arch Neurol. 2003. PMID: 12975302

8

Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection.

Mantripragada KK, Buckley PG, Jarbo C, Menzel U, Dumanski JP. Mantripragada KK, et al. J Mol Med (Berl). 2003 Jul;81(7):443-51. doi: 10.1007/s00109-003-0458-3. Epub 2003 Jun 27. J Mol Med (Berl). 2003. PMID: 12830322

9

Genomic EcoRI polymorphism and cosmid sequencing reveal an insertion/deletion and a new IGLV5 allele in the human immunoglobulin lambda variable locus (22q11.2/IGLV).

Moraes Junta C, Passos GA. Moraes Junta C, et al. Immunogenetics. 2003 Apr;55(1):10-5. doi: 10.1007/s00251-003-0549-x. Epub 2003 Mar 29. Immunogenetics. 2003. PMID: 12679855

10

High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH.

Mantripragada KK, Buckley PG, Benetkiewicz M, De Bustos C, Hirvelä C, Jarbo C, Bruder CE, Wensman H, Mathiesen T, Nyberg G, Papi L, Collins VP, Ichimura K, Evans G, Dumanski JP. Mantripragada KK, et al. Int J Oncol. 2003 Mar;22(3):615-22. Int J Oncol. 2003. PMID: 12579316

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