Similar articles for PMID: 7697714

Year	Number of Results
1987	2
1991	3
1992	9
1993	5
1994	5
1995	7
1996	10
1997	8
1998	3
1999	6
2000	7
2001	2
2002	1
2003	1
2004	2
2005	8
2006	8
2007	2
2008	2
2009	5
2010	3
2011	6
2012	1
2013	4
2014	2
2015	3
2016	2
2017	3
2019	2
2020	4
2021	4
2022	1
2024	0

1

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome).

Gibbons RJ, Picketts DJ, Villard L, Higgs DR. Gibbons RJ, et al. Cell. 1995 Mar 24;80(6):837-45. doi: 10.1016/0092-8674(95)90287-2. Cell. 1995. PMID: 7697714 Free article.

2

A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome.

Ion A, Telvi L, Chaussain JL, Galacteros F, Valayer J, Fellous M, McElreavey K. Ion A, et al. Am J Hum Genet. 1996 Jun;58(6):1185-91. Am J Hum Genet. 1996. PMID: 8651295 Free PMC article.

3

Syndromal mental retardation due to mutations in a regulator of gene expression.

Gibbons RJ, Picketts DJ, Higgs DR. Gibbons RJ, et al. Hum Mol Genet. 1995;4 Spec No:1705-9. doi: 10.1093/hmg/4.suppl_1.1705. Hum Mol Genet. 1995. PMID: 8541868 Review.

4

Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemia.

Villard L, Toutain A, Lossi AM, Gecz J, Houdayer C, Moraine C, Fontès M. Villard L, et al. Am J Hum Genet. 1996 Mar;58(3):499-505. Am J Hum Genet. 1996. PMID: 8644709 Free PMC article.

5

A point mutation in the XNP gene, associated with an ATR-X phenotype without alpha-thalassemia.

Villard L, Lacombe D, Fontés M. Villard L, et al. Eur J Hum Genet. 1996;4(6):316-20. doi: 10.1159/000472225. Eur J Hum Genet. 1996. PMID: 9043863

6

Molecular genetic study of japanese patients with X-linked alpha-thalassemia/mental retardation syndrome (ATR-X).

Wada T, Kubota T, Fukushima Y, Saitoh S. Wada T, et al. Am J Med Genet. 2000 Sep 18;94(3):242-8. Am J Med Genet. 2000. PMID: 10995512

7

Alpha-thalassemia/mental retardation syndrome, X-Linked (ATR-X, MIM #301040, ATR-X/XNP/XH2 gene MIM #300032).

Villard L, Fontes M. Villard L, et al. Eur J Hum Genet. 2002 Apr;10(4):223-5. doi: 10.1038/sj.ejhg.5200800. Eur J Hum Genet. 2002. PMID: 12032728 No abstract available.

8

Molecular-clinical spectrum of the ATR-X syndrome.

Gibbons RJ, Higgs DR. Gibbons RJ, et al. Am J Med Genet. 2000 Fall;97(3):204-12. doi: 10.1002/1096-8628(200023)97:3<204::AID-AJMG1038>3.0.CO;2-X. Am J Med Genet. 2000. PMID: 11449489 Review.

9

The alpha-thalassemia/mental retardation syndromes.

Gibbons RJ, Higgs DR. Gibbons RJ, et al. Medicine (Baltimore). 1996 Mar;75(2):45-52. doi: 10.1097/00005792-199603000-00001. Medicine (Baltimore). 1996. PMID: 8606626 Free article. Review.

10

ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.

Picketts DJ, Higgs DR, Bachoo S, Blake DJ, Quarrell OW, Gibbons RJ. Picketts DJ, et al. Hum Mol Genet. 1996 Dec;5(12):1899-907. doi: 10.1093/hmg/5.12.1899. Hum Mol Genet. 1996. PMID: 8968741

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