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Items: 7

1.

Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism.

Martin CL, Duvall JA, Ilkin Y, Simon JS, Arreaza MG, Wilkes K, Alvarez-Retuerto A, Whichello A, Powell CM, Rao K, Cook E, Geschwind DH.

Am J Med Genet B Neuropsychiatr Genet. 2007 Oct 5;144B(7):869-76.

PMID:
17503474
2.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
3.

Orchestration of neurodevelopmental programs by RBFOX1: implications for autism spectrum disorder.

Bill BR, Lowe JK, Dybuncio CT, Fogel BL.

Int Rev Neurobiol. 2013;113:251-67. doi: 10.1016/B978-0-12-418700-9.00008-3. Review.

4.

Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH.

Goizet C, Excoffier E, Taine L, Taupiac E, El Moneim AA, Arveiler B, Bouvard M, Lacombe D.

Am J Med Genet. 2000 Dec 4;96(6):839-44. Review.

PMID:
11121193
5.

Autism and cytogenetic abnormalities: solving autism one chromosome at a time.

Martin CL, Ledbetter DH.

Curr Psychiatry Rep. 2007 Apr;9(2):141-7. Review.

PMID:
17389126
6.

A case with a ring chromosome 13 in a cohort of 203 children with non-syndromic autism and review of the cytogenetic literature.

Charalsawadi C, Maisrikhaw W, Praphanphoj V, Wirojanan J, Hansakunachai T, Roongpraiwan R, Sombuntham T, Ruangdaraganon N, Limprasert P.

Cytogenet Genome Res. 2014;144(1):1-8. doi: 10.1159/000365909. Review.

PMID:
25171325
7.

Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist.

Lintas C, Persico AM.

J Med Genet. 2009 Jan;46(1):1-8. doi: 10.1136/jmg.2008.060871. Review.

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