Format
Sort by
Items per page

Send to

Choose Destination

Links from Books

Items: 9

1.

A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.

Gilling M, Lauritsen MB, Møller M, Henriksen KF, Vicente A, Oliveira G, Cintin C, Eiberg H, Andersen PS, Mors O, Rosenberg T, Brøndum-Nielsen K, Cotterill RM, Lundsteen C, Ropers HH, Ullmann R, Bache I, Tümer Z, Tommerup N.

Eur J Hum Genet. 2008 Mar;16(3):312-9. doi: 10.1038/sj.ejhg.5201985. Epub 2008 Jan 9.

2.

Long-term survival in a patient with del(18)(q12.2q21.1).

Tinkle BT, Christianson CA, Schorry EK, Webb T, Hopkin RJ.

Am J Med Genet A. 2003 May 15;119A(1):66-70.

PMID:
12707962
3.
4.

Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.

Hsu LY, Yu MT, Richkind KE, Van Dyke DL, Crandall BF, Saxe DF, Khodr GS, Mennuti M, Stetten G, Miller WA, Priest JH.

Prenat Diagn. 1996 Jan;16(1):1-28.

PMID:
8821848
5.

Trisomy 18q-. Trisomy mapping of chromosome 18 revisited.

Turleau C, Chavin-Colin F, Narbouton R, Asensi D, de Grouchy J.

Clin Genet. 1980 Jul;18(1):20-6.

PMID:
7418250
6.

Thymus deficiency in an infant with a chromosome t(18;22)(q12.2;p11.2)pat rearrangement.

Bowen P, Pabst H, Berry D, Collins-Nakai R, Hoo JJ.

Clin Genet. 1986 Feb;29(2):174-7.

PMID:
3955871
7.

Prenatal diagnosis of mosaicism for del(18)(q12.2q21.1) and a normal cell line.

Wilson MG, Lin MS.

J Med Genet. 1988 Sep;25(9):635-6. No abstract available.

8.

Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46,XY/46,XY,-18,+dic(18)(q12.2]).

Bryke CR, Lindgren V, Fryburg JS, Yang-Feng TL.

Am J Med Genet. 1990 Jun;36(2):247-50.

PMID:
2368814
9.

Another paracentric inversion of chromosome 18.

Bell J, Dunlop R, Bryan J.

Am J Med Genet. 1991 May 1;39(2):238. No abstract available.

PMID:
2063935

Supplemental Content

Support Center