Diagnosis of genetic abnormalities in developmenta... [Am J Med Genet A. 2007]

Related citations

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more? [Am J Med Genet A. 2005]
Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?
Bejjani BA, Saleki R, Ballif BC, Rorem EA, Sundin K, Theisen A, Kashork CD, Shaffer LG. Am J Med Genet A. 2005 Apr 30; 134(3):259-67.
Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases. [Am J Med Genet A. 2008]
Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.
Shao L, Shaw CA, Lu XY, Sahoo T, Bacino CA, Lalani SR, Stankiewicz P, Yatsenko SA, Li Y, Neill S, et al. Am J Med Genet A. 2008 Sep 1; 146A(17):2242-51.
Development and validation of a CGH microarray for clinical cytogenetic diagnosis. [Genet Med. 2005]
Development and validation of a CGH microarray for clinical cytogenetic diagnosis.
Cheung SW, Shaw CA, Yu W, Li J, Ou Z, Patel A, Yatsenko SA, Cooper ML, Furman P, Stankiewicz P, et al. Genet Med. 2005 Jul-Aug; 7(6):422-32.
Review [Diagnosis of cryptic chromosome aberrations] [Tidsskr Nor Laegeforen. 2003]
Review [Diagnosis of cryptic chromosome aberrations]
Ness GO, Houge G. Tidsskr Nor Laegeforen. 2003 Sep 11; 123(17):2418-21.
Review 22q13 deletion syndrome: an update and review for the primary pediatrician. [Clin Pediatr (Phila). 2004]
Review 22q13 deletion syndrome: an update and review for the primary pediatrician.
Havens JM, Visootsak J, Phelan MC, Graham JM Jr. Clin Pediatr (Phila). 2004 Jan-Feb; 43(1):43-53.

See reviews... See all...

Cited by 2 PubMed Central articles

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant. [J Med Genet. 2009]
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.
Hannes FD, Sharp AJ, Mefford HC, de Ravel T, Ruivenkamp CA, Breuning MH, Fryns JP, Devriendt K, Van Buggenhout G, Vogels A, et al. J Med Genet. 2009 Apr; 46(4):223-32. Epub 2008 Jun 11.
Submicroscopic chromosome imbalance in patients with developmental delay and/or dysmorphism referred specifically for Fragile X testing and karyotype analysis. [Mol Cytogenet. 2008]
Submicroscopic chromosome imbalance in patients with developmental delay and/or dysmorphism referred specifically for Fragile X testing and karyotype analysis.
Ahn JW, Mann K, Docherty Z, Mackie Ogilvie C. Mol Cytogenet. 2008 Mar 26; 1:2. Epub 2008 Mar 26.

All links from this record

Related Citations
Calculated set of PubMed citations closely related to the selected article(s) retrieved using a word weight algorithm. Related articles are displayed in ranked order from most to least relevant, with the “linked from” citation displayed first.
Cited in PMC
Full-text articles in the PubMed Central Database that cite the current articles.

Recent activity

Clear Turn Off Turn On

Diagnosis of genetic abnormalities in developmentally delayed patients: a new st...
Diagnosis of genetic abnormalities in developmentally delayed patients: a new strategy combining MLPA and array-CGH.
Am J Med Genet A. 2007 Mar 15 ;143(6):610-4.

PubMed
An analphoid supernumerary marker chromosome derived from chromosome 3 ascertain...
An analphoid supernumerary marker chromosome derived from chromosome 3 ascertained in a fetus with multiple malformations.
J Med Genet. 2000 Oct ;37(10):807-10.

PubMed
On the origin of trisomy 21 Down syndrome.
On the origin of trisomy 21 Down syndrome.
Mol Cytogenet. 2008 Sep 18 ;1:21.

PubMed
Detailed molecular and clinical investigation of a child with a partial deletion...
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome).
Mol Cytogenet. 2009 Dec 9 ;2:26.

PubMed
Routine use of methods for improved G-band resolution in a population of patient...
Routine use of methods for improved G-band resolution in a population of patients with malformations and developmental delay.
Am J Med Genet. 1991 Jan ;38(1):37-42.

PubMed

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

PubMed

Display Settings:

Send to:

Diagnosis of genetic abnormalities in developmentally delayed patients: a new strategy combining MLPA and array-CGH.

Publication Types, MeSH Terms

Publication Types:

MeSH Terms:

LinkOut - more resources

Full Text Sources:

Other Literature Sources:

Medical:

Libraries:

Supplemental Content

Related citations

Cited by 2 PubMed Central articles

All links from this record

Recent activity

Simple NCBI Directory

Getting Started

Resources

Popular

Featured

NCBI Information