PubMed (cited) for id: 141750

Year	Number of Results
1970	1
1981	1
1982	1
1984	1
1988	1
1989	1
1990	2
1993	1
1995	1
1997	2
1999	1
2000	2
2005	1
2007	1
2008	1
2024	0

1

Phenotype-genotype characterization of alpha-thalassemia mental retardation syndrome due to isolated monosomy of 16p13.3.

Gibson WT, Harvard C, Qiao Y, Somerville MJ, Lewis ME, Rajcan-Separovic E. Gibson WT, et al. Am J Med Genet A. 2008 Jan 15;146A(2):225-32. doi: 10.1002/ajmg.a.32056. Am J Med Genet A. 2008. PMID: 18076105

2

Refinement of the genetic cause of ATR-16.

Harteveld CL, Kriek M, Bijlsma EK, Erjavec Z, Balak D, Phylipsen M, Voskamp A, di Capua E, White SJ, Giordano PC. Harteveld CL, et al. Hum Genet. 2007 Nov;122(3-4):283-92. doi: 10.1007/s00439-007-0399-y. Epub 2007 Jun 28. Hum Genet. 2007. PMID: 17598130

3

ATR-16 due to a de novo complex rearrangement of chromosome 16.

Gallego MS, Zelaya G, Feliu AS, Rossetti L, Shaffer LG, Bailey KA, Bacino CA, Barreiro CZ. Gallego MS, et al. Hemoglobin. 2005;29(2):141-50. Hemoglobin. 2005. PMID: 15921166

4

The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome.

Pfeifer D, Poulat F, Holinski-Feder E, Kooy F, Scherer G. Pfeifer D, et al. Genomics. 2000 Jan 1;63(1):108-16. doi: 10.1006/geno.1999.6060. Genomics. 2000. PMID: 10662550

5

Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).

Holinski-Feder E, Reyniers E, Uhrig S, Golla A, Wauters J, Kroisel P, Bossuyt P, Rost I, Jedele K, Zierler H, Schwab S, Wildenauer D, Speicher MR, Willems PJ, Meitinger T, Kooy RF. Holinski-Feder E, et al. Am J Hum Genet. 2000 Jan;66(1):16-25. doi: 10.1086/302703. Am J Hum Genet. 2000. PMID: 10631133 Free PMC article.

6

Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres.

Slavotinek A, Rosenberg M, Knight S, Gaunt L, Fergusson W, Killoran C, Clayton-Smith J, Kingston H, Campbell RH, Flint J, Donnai D, Biesecker L. Slavotinek A, et al. J Med Genet. 1999 May;36(5):405-11. J Med Genet. 1999. PMID: 10353788 Free PMC article.

7

De novo 16p deletion: ATR-16 syndrome.

Lindor NM, Valdes MG, Wick M, Thibodeau SN, Jalal S. Lindor NM, et al. Am J Med Genet. 1997 Nov 12;72(4):451-4. Am J Med Genet. 1997. PMID: 9375730

8

Molecular-cytogenetic detection of a deletion of 1p36.3.

Giraudeau F, Aubert D, Young I, Horsley S, Knight S, Kearney L, Vergnaud G, Flint J. Giraudeau F, et al. J Med Genet. 1997 Apr;34(4):314-7. doi: 10.1136/jmg.34.4.314. J Med Genet. 1997. PMID: 9138156 Free PMC article.

9

De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16).

Lamb J, Harris PC, Wilkie AO, Wood WG, Dauwerse JG, Higgs DR. Lamb J, et al. Am J Hum Genet. 1993 Apr;52(4):668-76. Am J Hum Genet. 1993. PMID: 8460633 Free PMC article.

10

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation.

Flint J, Wilkie AO, Buckle VJ, Winter RM, Holland AJ, McDermid HE. Flint J, et al. Nat Genet. 1995 Feb;9(2):132-40. doi: 10.1038/ng0295-132. Nat Genet. 1995. PMID: 7719339

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