Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 15

1.

Autism and maternally derived aberrations of chromosome 15q.

Schroer RJ, Phelan MC, Michaelis RC, Crawford EC, Skinner SA, Cuccaro M, Simensen RJ, Bishop J, Skinner C, Fender D, Stevenson RE.

Am J Med Genet. 1998 Apr 1;76(4):327-36.

PMID:
9545097
2.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
3.

The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders.

Bolton PF, Dennis NR, Browne CE, Thomas NS, Veltman MW, Thompson RJ, Jacobs P.

Am J Med Genet. 2001 Dec 8;105(8):675-85. Review.

PMID:
11803514
4.

Deletion of chromosome 2q37 and autism: a distinct subtype?

Ghaziuddin M, Burmeister M.

J Autism Dev Disord. 1999 Jun;29(3):259-63. Review.

PMID:
10425588
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.

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
7.

[Autism, chromosome 15 and the GAbaergic dysfunction hypothesis].

Solís-Añez E, Delgado-Luengo W, Hernández ML.

Invest Clin. 2007 Dec;48(4):529-41. Review. Spanish.

PMID:
18271397
8.

The molecular genetics of autism.

Wassink TH, Piven J.

Curr Psychiatry Rep. 2000 Apr;2(2):170-5. Review.

PMID:
11122951
9.

Intersitial deletion of 20p: new candidate region for Hirschsprung disease and autism?

Michaelis RC, Skinner SA, Deason R, Skinner C, Moore CL, Phelan MC.

Am J Med Genet. 1997 Aug 22;71(3):298-304. Review.

PMID:
9268100
10.

The genetics of autism.

Spence MA.

Curr Opin Pediatr. 2001 Dec;13(6):561-5. Review.

PMID:
11753107
11.

Epigenetics of autism spectrum disorders.

Schanen NC.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R138-50. Review.

12.

Unrelated patients with a rearrangement of chromosome 2 causing duplication of 2p23 and deletion of 2q37.

Armstrong L, Allanson JE, Weaver DD, Bevan CJ, Hobart HH.

Am J Med Genet A. 2005 Apr 30;134(3):299-304. Review.

PMID:
15742366
13.

Autism: the paediatric neurologist's tale.

McKinlay I.

Br J Disord Commun. 1989 Aug;24(2):201-7. Review.

PMID:
2690919
14.

The role of new genetic technology in investigating autism and developmental delay.

Shur N, Gunn S, Feit L, Oh AK, Yatchmink Y, Abuelo D.

Med Health R I. 2011 May;94(5):131, 134-7. Review. No abstract available.

PMID:
21710921
15.

De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: a case report and literature review.

Jolley A, Corbett M, McGregor L, Waters W, Brown S, Nicholl J, Yu S.

Am J Med Genet A. 2013 Jun;161A(6):1508-12. doi: 10.1002/ajmg.a.35922. Review. No abstract available.

PMID:
23650183
Items per page

Supplemental Content

Support Center