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Items: 1 to 20 of 110

1.

Autistic symptoms among children and young adults with isodicentric chromosome 15.

Rineer S, Finucane B, Simon EW.

Am J Med Genet. 1998 Sep 7;81(5):428-33.

PMID:
9754629
2.

Autistic symptoms among children and young adults with isodicentric chromosome 15.

Wolpert C, Pericak-Vance MA, Abramson RK, Wright HH, Cuccaro ML.

Am J Med Genet. 2000 Feb 7;96(1):128-9. No abstract available.

PMID:
10686566
3.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
4.

Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports.

Simic M, Turk J.

Eur Child Adolesc Psychiatry. 2004 Dec;13(6):389-93.

PMID:
15619052
5.

Autism associated with marker chromosome.

Gillberg C, Steffenburg S, Wahlström J, Gillberg IC, Sjöstedt A, Martinsson T, Liedgren S, Eeg-Olofsson O.

J Am Acad Child Adolesc Psychiatry. 1991 May;30(3):489-94.

PMID:
2055888
6.

Autistic symptoms in isodicentric 15 syndrome: response to Wolpert et al.

Simon EW, Finucane B, Rineer S.

Am J Med Genet. 2000 Jun 12;96(3):432-3. No abstract available.

PMID:
10898930
7.

Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disorders.

Vorsanova SG, Yurov IY, Demidova IA, Voinova-Ulas VY, Kravets VS, Solov'ev IV, Gorbachevskaya NL, Yurov YB.

Neurosci Behav Physiol. 2007 Jul;37(6):553-8.

PMID:
17657425
8.

Y chromosome haplogroups in autistic subjects.

Jamain S, Quach H, Quintana-Murci L, Betancur C, Philippe A, Gillberg C, Sponheim E, Skjeldal OH, Fellous M, Leboyer M, Bourgeron T.

Mol Psychiatry. 2002;7(2):217-9.

9.

Genetics of childhood disorders: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism.

Sutcliffe JS, Nurmi EL, Lombroso PJ.

J Am Acad Child Adolesc Psychiatry. 2003 Feb;42(2):253-6. No abstract available.

PMID:
12544187
10.

Three probands with autistic disorder and isodicentric chromosome 15.

Wolpert CM, Menold MM, Bass MP, Qumsiyeh MB, Donnelly SL, Ravan SA, Vance JM, Gilbert JR, Abramson RK, Wright HH, Cuccaro ML, Pericak-Vance MA.

Am J Med Genet. 2000 Jun 12;96(3):365-72. Review.

PMID:
10898916
11.

Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.

Philippi A, Tores F, Carayol J, Rousseau F, Letexier M, Roschmann E, Lindenbaum P, Benajjou A, Fontaine K, Vazart C, Gesnouin P, Brooks P, Hager J.

BMC Med Genet. 2007 Dec 6;8:74.

12.

A longitudinal follow-up study of autistic symptoms in children and adults with duplications of 15q11-13.

Simon EW, Haas-Givler B, Finucane B.

Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):463-467. doi: 10.1002/ajmg.b.31000.

PMID:
19548260
13.

Chromosomal abnormalities in a series of children with autistic disorder.

Konstantareas MM, Homatidis S.

J Autism Dev Disord. 1999 Aug;29(4):275-85.

PMID:
10478727
14.

Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region.

Kwasnicka-Crawford DA, Roberts W, Scherer SW.

J Autism Dev Disord. 2007 Apr;37(4):694-702.

PMID:
17006779
15.

15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.

Koochek M, Harvard C, Hildebrand MJ, Van Allen M, Wingert H, Mickelson E, Holden JJ, Rajcan-Separovic E, Lewis ME.

Clin Genet. 2006 Feb;69(2):124-34.

PMID:
16433693
16.

Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders.

Keller K, Williams C, Wharton P, Paulk M, Bent-Williams A, Gray B, Ward A, Stalker H, Wallace M, Carter R, Zori R.

Am J Med Genet A. 2003 Mar 1;117A(2):105-11.

PMID:
12567405
17.

Association between a GABRB3 polymorphism and autism.

Buxbaum JD, Silverman JM, Smith CJ, Greenberg DA, Kilifarski M, Reichert J, Cook EH Jr, Fang Y, Song CY, Vitale R.

Mol Psychiatry. 2002;7(3):311-6.

19.

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
20.

Association study of the commonly recognized breakpoints in chromosome 15q11-q13 in Japanese autistic patients.

Kato C, Tochigi M, Koishi S, Kawakubo Y, Yamamoto K, Matsumoto H, Hashimoto O, Kim SY, Watanabe K, Kano Y, Nanba E, Kato N, Sasaki T.

Psychiatr Genet. 2008 Jun;18(3):133-6. doi: 10.1097/YPG.0b013e3282fb0064.

PMID:
18496211

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