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Items: 1 to 20 of 105

1.

The early origins of autism.

Rodier PM.

Sci Am. 2000 Feb;282(2):56-63. Review. No abstract available.

PMID:
10710787
2.

No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD).

Talebizadeh Z, Bittel DC, Miles JH, Takahashi N, Wang CH, Kibiryeva N, Butler MG.

J Med Genet. 2002 Nov;39(11):e70. No abstract available.

3.

Development. New hints into the biological basis of autism.

Stokstad E.

Science. 2001 Oct 5;294(5540):34-7. No abstract available.

PMID:
11588233
4.
5.

Infantile autism in monozygotic twins.

Salimi-Eshkevari H.

J Am Acad Child Psychiatry. 1985 Sep;24(5):643-6. No abstract available.

PMID:
4045065
6.

[Early infantile autism in twins (review)].

Moskalenko VD.

Zh Nevropatol Psikhiatr Im S S Korsakova. 1979;79(10):1435-41. Review. Russian. No abstract available.

PMID:
386670
7.

Genetic influences and infantile autism.

Folstein S, Rutter M.

Nature. 1977 Feb 24;265(5596):726-8. No abstract available.

PMID:
558516
8.

Monozygotic twins concordant for infantile autism: follow-up.

Campbell M, Dominijanni C, Schneider B.

Br J Psychiatry. 1977 Dec;131:616-22.

PMID:
563753
9.

Lack of association of HOXA1 and HOXB1 variants with autism in the Indian population.

Sen B, Sinha S, Ahmed S, Ghosh S, Gangopadhyay PK, Usha R.

Psychiatr Genet. 2007 Feb;17(1):1. No abstract available.

PMID:
17167333
10.

Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients.

Romano V, Calì F, Mirisola M, Gambino G, D' Anna R, Di Rosa P, Seidita G, Chiavetta V, Aiello F, Canziani F, De Leo G, Ayala GF, Elia M.

Mol Psychiatry. 2003 Aug;8(8):716-7. No abstract available.

PMID:
12888798
11.

Autism and epilepsy: organic connections?

Lenti C.

J Am Acad Child Adolesc Psychiatry. 1992 Mar;31(2):370. No abstract available.

PMID:
1564042
12.

A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea.

Rossi E, Verri AP, Patricelli MG, Destefani V, Ricca I, Vetro A, Ciccone R, Giorda R, Toniolo D, Maraschio P, Zuffardi O.

Eur J Med Genet. 2008 Nov-Dec;51(6):631-8. doi: 10.1016/j.ejmg.2008.06.010. Epub 2008 Jul 16.

PMID:
18675947
13.

No association between the EN2 gene and autistic disorder.

Zhong H, Serajee FJ, Nabi R, Huq AH.

J Med Genet. 2003 Jan;40(1):e4. No abstract available.

14.

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families.

Li J, Tabor HK, Nguyen L, Gleason C, Lotspeich LJ, Spiker D, Risch N, Myers RM.

Am J Med Genet. 2002 Jan 8;114(1):24-30.

PMID:
11840501
15.

Expansion of the ARX spectrum.

Wallerstein R, Sugalski R, Cohn L, Jawetz R, Friez M.

Clin Neurol Neurosurg. 2008 Jun;110(6):631-4. doi: 10.1016/j.clineuro.2008.03.007. Epub 2008 May 6.

PMID:
18462864
16.

Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders.

Ingram JL, Stodgell CJ, Hyman SL, Figlewicz DA, Weitkamp LR, Rodier PM.

Teratology. 2000 Dec;62(6):393-405.

PMID:
11091361
17.

No association between allelic variants of HOXA1/HOXB1 and autism.

Gallagher L, Hawi Z, Kearney G, Fitzgerald M, Gill M.

Am J Med Genet B Neuropsychiatr Genet. 2004 Jan 1;124B(1):64-7.

PMID:
14681917
18.

No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.

Devlin B, Bennett P, Cook EH Jr, Dawson G, Gonen D, Grigorenko EL, McMahon W, Pauls D, Smith M, Spence MA, Schellenberg GD; Collaborative Programs of Excellence in Autism (CPEA) Genetics Network.

Am J Med Genet. 2002 Aug 8;114(6):667-72.

19.

Monozygotic twins with tuberous sclerosis discordant for the severity of developmental deficits.

Humphrey A, Higgins JN, Yates JR, Bolton PF.

Neurology. 2004 Mar 9;62(5):795-8. Erratum in: Neurology. 2004 Nov 9;63(9):1764.

PMID:
15007135
20.

Technical note: are perinatal complications causes or consequences of autism?

Goodman R.

J Child Psychol Psychiatry. 1990 Jul;31(5):809-12. No abstract available.

PMID:
2398123

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