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Items: 1 to 20 of 25

1.

Genomic imprinting and Turner syndrome.

Bondy CA, Hougen HY, Zhou J, Cheng CM.

Pediatr Endocrinol Rev. 2012 May;9 Suppl 2:728-32. Review.

PMID:
22946286
2.

Cognition and the sex chromosomes: studies in Turner syndrome.

Ross J, Roeltgen D, Zinn A.

Horm Res. 2006;65(1):47-56. Epub 2006 Jan 4. Review.

3.

Molecular analysis of genes on Xp controlling Turner syndrome and premature ovarian failure (POF).

Zinn AR, Ross JL.

Semin Reprod Med. 2001 Jun;19(2):141-6. Review.

PMID:
11480911
4.

[Turner's syndrome--correlation between karyotype and phenotype].

Lacka K.

Endokrynol Pol. 2005 Nov-Dec;56(6):986-93. Review. Polish.

PMID:
16821224
5.

Imprinting of the mouse Igf2r gene depends on an intronic CpG island.

Wutz A, Barlow DP.

Mol Cell Endocrinol. 1998 May 25;140(1-2):9-14. Review.

PMID:
9722161
6.

Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: implications for the mechanism leading to generation of a 45,X karyotype.

Uematsu A, Yorifuji T, Muroi J, Kawai M, Mamada M, Kaji M, Yamanaka C, Momoi T, Nakahata T.

Am J Med Genet. 2002 Aug 1;111(2):134-9. Review.

PMID:
12210339
7.

The conflict theory of genomic imprinting: how much can be explained?

Iwasa Y.

Curr Top Dev Biol. 1998;40:255-93. Review.

PMID:
9673853
8.

Genomic imprinting on the X chromosome: implications for brain and behavioral phenotypes.

Davies W.

Ann N Y Acad Sci. 2010 Sep;1204 Suppl:E14-9. doi: 10.1111/j.1749-6632.2010.05567.x. Review.

PMID:
20840165
9.

Social cognition in Turner's Syndrome.

Burnett AC, Reutens DC, Wood AG.

J Clin Neurosci. 2010 Mar;17(3):283-6. doi: 10.1016/j.jocn.2009.09.006. Epub 2010 Jan 20. Review.

PMID:
20089410
10.

The 39,XO mouse as a model for the neurobiology of Turner syndrome and sex-biased neuropsychiatric disorders.

Lynn PM, Davies W.

Behav Brain Res. 2007 May 16;179(2):173-82. Epub 2007 Feb 20. Review.

PMID:
17367875
11.

Neurodevelopmental and psychosocial aspects of Turner syndrome.

Ross J, Zinn A, McCauley E.

Ment Retard Dev Disabil Res Rev. 2000;6(2):135-41. Review.

PMID:
10899807
13.

X-linked genes and mental functioning.

Skuse DH.

Hum Mol Genet. 2005 Apr 15;14 Spec No 1:R27-32. Review.

14.

Turner syndrome: the case of the missing sex chromosome.

Zinn AR, Page DC, Fisher EM.

Trends Genet. 1993 Mar;9(3):90-3. Review.

PMID:
8488568
15.

Sexual dimorphism in parental imprint ontogeny and contribution to embryonic development.

Bourc'his D, Proudhon C.

Mol Cell Endocrinol. 2008 Jan 30;282(1-2):87-94. doi: 10.1016/j.mce.2007.11.025. Epub 2007 Nov 29. Review.

PMID:
18178305
16.

Genomic imprinting in fetal growth and development.

Hitchins MP, Moore GE.

Expert Rev Mol Med. 2002 May 9;4(11):1-19. Review.

PMID:
14987379
17.

Genes and social skills.

Scourfield J, McGuffin P, Thapar A.

Bioessays. 1997 Dec;19(12):1125-7. Review.

PMID:
9423351
18.

The role of imprinted genes in fetal growth.

Miozzo M, Simoni G.

Biol Neonate. 2002;81(4):217-28. Review.

PMID:
12011565
19.

X-linked premature ovarian failure: a complex disease.

Toniolo D.

Curr Opin Genet Dev. 2006 Jun;16(3):293-300. Epub 2006 May 2. Review.

PMID:
16650756
20.

[Turner syndrome and mosaicism].

Battin J.

Bull Acad Natl Med. 2003;187(2):359-67; discussion 368-70. Review. French.

PMID:
14556446
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