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Results: 1 to 20 of 86

1.

Interpretation of clonality and X-chromosome inactivation assays urge attention.

Gomes CC, Gomez RS.

J Clin Pathol. 2012 May;65(5):473. doi: 10.1136/jclinpath-2011-200526. Epub 2011 Nov 22. No abstract available.

PMID:
22110157
[PubMed - indexed for MEDLINE]
2.

X-linked clonality testing: interpretation and limitations.

Chen GL, Prchal JT.

Blood. 2007 Sep 1;110(5):1411-9. Epub 2007 Apr 13. Review.

PMID:
17435115
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Phenotype in X chromosome rearrangements: pitfalls of X inactivation study.

Schluth C, Cossée M, Girard-Lemaire F, Carelle N, Dollfus H, Jeandidier E, Flori E.

Pathol Biol (Paris). 2007 Feb;55(1):29-36. Epub 2006 May 11.

PMID:
16690229
[PubMed - indexed for MEDLINE]
4.

Female Hunter syndrome caused by a single mutation and familial XCI skewing: implications for other X-linked disorders.

Kloska A, Jakóbkiewicz-Banecka J, Tylki-Szymańska A, Czartoryska B, Węgrzyn G.

Clin Genet. 2011 Nov;80(5):459-65. doi: 10.1111/j.1399-0004.2010.01574.x. Epub 2010 Nov 10.

PMID:
21062272
[PubMed - indexed for MEDLINE]
5.

X chromosome inactivation in Rett Syndrome and its correlations with MECP2 mutations and phenotype.

Xinhua Bao, Shengling Jiang, Fuying Song, Hong Pan, Meirong Li, Wu XR.

J Child Neurol. 2008 Jan;23(1):22-5. doi: 10.1177/0883073807307077.

PMID:
18184939
[PubMed - indexed for MEDLINE]
6.

Why females are mosaics, X-chromosome inactivation, and sex differences in disease.

Migeon BR.

Gend Med. 2007 Jun;4(2):97-105.

PMID:
17707844
[PubMed - indexed for MEDLINE]
7.

Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25.

Macedo-Souza LI, Kok F, Santos S, Licinio L, Lezirovitz K, Nascimento RM, Bueno C, Martyn M, Leão EK, Zatz M.

Neurogenetics. 2008 Jul;9(3):225-6. doi: 10.1007/s10048-008-0130-8. Epub 2008 May 8. No abstract available.

PMID:
18463901
[PubMed - indexed for MEDLINE]
8.

X chromosome inactivation in clinical practice.

Orstavik KH.

Hum Genet. 2009 Sep;126(3):363-73. doi: 10.1007/s00439-009-0670-5. Epub 2009 Apr 25. Review.

PMID:
19396465
[PubMed - indexed for MEDLINE]
9.

Genetics and epigenetics of the X chromosome.

Morey C, Avner P.

Ann N Y Acad Sci. 2010 Dec;1214:E18-33. doi: 10.1111/j.1749-6632.2010.05943.x. Review.

PMID:
21382199
[PubMed - indexed for MEDLINE]
10.

Strong purifying selection at genes escaping X chromosome inactivation.

Park C, Carrel L, Makova KD.

Mol Biol Evol. 2010 Nov;27(11):2446-50. doi: 10.1093/molbev/msq143. Epub 2010 Jun 9.

PMID:
20534706
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

[Infrequent X chromosome abnormality and X-linked syndromic deafness].

Wang YJ, Shi XL, Nie JW, Ni B, Yin ZC, Dai HP.

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2004 Oct;29(5):500-3. Chinese.

PMID:
16137031
[PubMed - indexed for MEDLINE]
Free Article
12.

Testing for association on the X chromosome.

Clayton D.

Biostatistics. 2008 Oct;9(4):593-600. doi: 10.1093/biostatistics/kxn007. Epub 2008 Apr 25.

PMID:
18441336
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

The relationship of x-linked primary immune deficiencies and autoimmunity.

Pessach IM.

Curr Allergy Asthma Rep. 2010 Sep;10(5):311-9. doi: 10.1007/s11882-010-0127-x. Review.

PMID:
20571932
[PubMed - indexed for MEDLINE]
14.

[Clonality study of palmar fibromatosis].

Wang L, Zhu HG.

Zhonghua Bing Li Xue Za Zhi. 2006 Apr;35(4):224-7. Chinese.

PMID:
16776980
[PubMed - indexed for MEDLINE]
15.

Clonality studies in sacral chordoma.

Klingler L, Trammell R, Allan DG, Butler MG, Schwartz HS.

Cancer Genet Cytogenet. 2006 Nov;171(1):68-71.

PMID:
17074594
[PubMed - indexed for MEDLINE]
16.

[X chromosome].

Verloes A.

Presse Med. 2007 Mar;36 Spec No 1:1S7-13. Review. French.

PMID:
17546761
[PubMed - indexed for MEDLINE]
17.

Brief report: non-random X chromosome inactivation in females with autism.

Talebizadeh Z, Bittel DC, Veatch OJ, Kibiryeva N, Butler MG.

J Autism Dev Disord. 2005 Oct;35(5):675-81.

PMID:
16167093
[PubMed - indexed for MEDLINE]
18.

Skewed X inactivation in healthy individuals and in different diseases.

Ørstavik KH.

Acta Paediatr Suppl. 2006 Apr;95(451):24-9. Review.

PMID:
16720461
[PubMed - indexed for MEDLINE]
19.

A novel locus for X-linked congenital cataract on Xq24.

Craig JE, Friend KL, Gecz J, Rattray KM, Troski M, Mackey DA, Burdon KP.

Mol Vis. 2008 Apr 18;14:721-6.

PMID:
18431456
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Discrimination of polycythemias and thrombocytoses by novel, simple, accurate clonality assays and comparison with PRV-1 expression and BFU-E response to erythropoietin.

Liu E, Jelinek J, Pastore YD, Guan Y, Prchal JF, Prchal JT.

Blood. 2003 Apr 15;101(8):3294-301. Epub 2002 Dec 19.

PMID:
12515724
[PubMed - indexed for MEDLINE]
Free Article

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