Display Settings:

Format
Sort by

Send to:

Choose Destination

Results: 4

1.

Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome.

Chen CP, Lin SP, Wang TH, Chen YJ, Chen M, Wang W.

Prenat Diagn. 2006 Aug;26(8):725-9.

PMID:
16927391
[PubMed - indexed for MEDLINE]
2.

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features.

Shaw-Smith C, Redon R, Rickman L, Rio M, Willatt L, Fiegler H, Firth H, Sanlaville D, Winter R, Colleaux L, Bobrow M, Carter NP.

J Med Genet. 2004 Apr;41(4):241-8.

PMID:
15060094
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation.

Piram A, Ortolan D, Peres LC, Pina-Neto JM, Riegel M, Schinzel A.

Am J Med Genet A. 2003 Jul 15;120A(2):247-52. Review.

PMID:
12833408
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk