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Items: 12

1.

Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.

Osbun N, Li J, O'Driscoll MC, Strominger Z, Wakahiro M, Rider E, Bukshpun P, Boland E, Spurrell CH, Schackwitz W, Pennacchio LA, Dobyns WB, Black GC, Sherr EH.

Am J Med Genet A. 2011 Aug;155A(8):1865-76. doi: 10.1002/ajmg.a.34081. Epub 2011 Jul 7.

PMID:
21739582
2.

Human brain imaging studies of DISC1 in schizophrenia, bipolar disorder and depression: a systematic review.

Duff BJ, Macritchie KA, Moorhead TW, Lawrie SM, Blackwood DH.

Schizophr Res. 2013 Jun;147(1):1-13. doi: 10.1016/j.schres.2013.03.015. Epub 2013 Apr 16. Review.

PMID:
23602339
3.

Agenesis of the corpus callosum associated with DiGeorge-velocardiofacial syndrome: a case report and review of the literature.

Kraynack NC, Hostoffer RW, Robin NH.

J Child Neurol. 1999 Nov;14(11):754-6. Review.

PMID:
10593557
4.

MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum.

Bader I, Decker E, Mayr JA, Lunzer V, Koch J, Boltshauser E, Sperl W, Pietsch P, Ertl-Wagner B, Bolz H, Bergmann C, Rittinger O.

Eur J Med Genet. 2016 Aug;59(8):386-91. doi: 10.1016/j.ejmg.2016.06.007. Epub 2016 Jul 1. Review.

PMID:
27377014
5.

Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.

Edwards TJ, Sherr EH, Barkovich AJ, Richards LJ.

Brain. 2014 Jun;137(Pt 6):1579-613. doi: 10.1093/brain/awt358. Epub 2014 Jan 28. Review.

6.

Agenesis of the corpus callosum: lessons from humans and mice.

Kamnasaran D.

Clin Invest Med. 2005 Oct;28(5):267-82. Review.

PMID:
16265999
7.

The proximal chromosome 14q microdeletion syndrome: delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature.

Torgyekes E, Shanske AL, Anyane-Yeboa K, Nahum O, Pirzadeh S, Blumfield E, Jobanputra V, Warburton D, Levy B.

Am J Med Genet A. 2011 Aug;155A(8):1884-96. doi: 10.1002/ajmg.a.34090. Epub 2011 Jul 8. Review.

PMID:
21744488
8.

A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum.

Genuardi M, Calvieri F, Tozzi C, Coslovi R, Neri G.

Clin Dysmorphol. 1994 Oct;3(4):292-6. Review.

PMID:
7894733
9.

Neuropsychological profile of agenesis of the corpus callosum: a systematic review.

Siffredi V, Anderson V, Leventer RJ, Spencer-Smith MM.

Dev Neuropsychol. 2013;38(1):36-57. doi: 10.1080/87565641.2012.721421. Review.

PMID:
23311314
10.

[Congenital malformations of the brain. 2: Malformations of the corpus callosum and holoprocencephalies].

Rummeny C, Ertl-Wagner B, Reiser MF.

Radiologe. 2003 Nov;43(11):925-33. Review. German.

PMID:
14628116
11.

Agenesis of the corpus callosum: clinical, neuroradiological and cytogenetic studies.

Serur D, Jeret JS, Wisniewski K.

Neuropediatrics. 1988 May;19(2):87-91. Review.

PMID:
2453812
12.

Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity.

Paul LK, Brown WS, Adolphs R, Tyszka JM, Richards LJ, Mukherjee P, Sherr EH.

Nat Rev Neurosci. 2007 Apr;8(4):287-99. Review.

PMID:
17375041

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