Similar articles for PMID: 16199540

Year	Number of Results
1991	1
1993	1
1994	1
1995	1
1996	1
1997	1
1998	2
2000	2
2001	4
2002	4
2003	4
2004	9
2005	13
2006	17
2007	14
2008	15
2009	11
2010	4
2011	2
2012	2
2013	4
2014	5
2015	2
2016	2
2017	2
2018	2
2022	1
2024	0

1

Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.

Ravnan JB, Tepperberg JH, Papenhausen P, Lamb AN, Hedrick J, Eash D, Ledbetter DH, Martin CL. Ravnan JB, et al. J Med Genet. 2006 Jun;43(6):478-89. doi: 10.1136/jmg.2005.036350. Epub 2005 Sep 30. J Med Genet. 2006. PMID: 16199540 Free PMC article.

2

Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH.

Joyce CA, Dennis NR, Cooper S, Browne CE. Joyce CA, et al. Hum Genet. 2001 Oct;109(4):440-51. doi: 10.1007/s004390100588. Hum Genet. 2001. PMID: 11702226

3

Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.

Riegel M, Baumer A, Jamar M, Delbecque K, Herens C, Verloes A, Schinzel A. Riegel M, et al. Hum Genet. 2001 Sep;109(3):286-94. doi: 10.1007/s004390100585. Hum Genet. 2001. PMID: 11702209

4

Frequency of truly cryptic subtelomere abnormalities--a study of 534 patients and literature review.

Yu S, Baker E, Hinton L, Eyre HJ, Waters W, Higgins S, Sutherland GR, Haan E. Yu S, et al. Clin Genet. 2005 Nov;68(5):436-41. doi: 10.1111/j.1399-0004.2005.00513.x. Clin Genet. 2005. PMID: 16207211 Review.

5

Detection of cryptic subtelomeric chromosome abnormalities and identification of anonymous chromatin using a quantitative multiplex ligation-dependent probe amplification (MLPA) assay.

Northrop EL, Ren H, Bruno DL, McGhie JD, Coffa J, Schouten J, Choo KH, Slater HR. Northrop EL, et al. Hum Mutat. 2005 Nov;26(5):477-86. doi: 10.1002/humu.20243. Hum Mutat. 2005. PMID: 16170807

6

FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype.

Baroncini A, Rivieri F, Capucci A, Croci G, Franchi F, Sensi A, Battaglia P, Aiello V, Calzolari E. Baroncini A, et al. Eur J Med Genet. 2005 Oct-Dec;48(4):388-96. doi: 10.1016/j.ejmg.2005.05.002. Eur J Med Genet. 2005. PMID: 16378923

7

Smith A, St Heaps L, Robson L. Smith A, et al. Am J Med Genet. 2002 Dec 15;113(4):346-50. doi: 10.1002/ajmg.10800. Am J Med Genet. 2002. PMID: 12457406

8

FISH analysis for apparently simple terminal deletions of the X chromosome: identification of hidden structural abnormalities.

Ogata T, Matsuo N, Fukushima Y, Saito M, Nose O, Miharu N, Uehara S, Ishizuka B. Ogata T, et al. Am J Med Genet. 2001 Dec 15;104(4):307-11. Am J Med Genet. 2001. PMID: 11754066

9

Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesis.

Iqbal MA, Ramadan S, Ali FA, Kurdi W. Iqbal MA, et al. Prenat Diagn. 2005 Dec;25(12):1142-9. doi: 10.1002/pd.1290. Prenat Diagn. 2005. PMID: 16240463

10

Genotype-phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the 'association des Cytogénéticiens de langue Française'.

Béri-Deixheimer M, Gregoire MJ, Toutain A, Brochet K, Briault S, Schaff JL, Leheup B, Jonveaux P. Béri-Deixheimer M, et al. Eur J Hum Genet. 2007 Apr;15(4):446-52. doi: 10.1038/sj.ejhg.5201784. Epub 2007 Feb 7. Eur J Hum Genet. 2007. PMID: 17290276

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