Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH

Intellectual disability (ID) affects about 3% of the population (IQ

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	American journal of medical genetics. Part A 2005-12, Vol.139A (3), p.173-185
Hauptverfasser:	Tyson, C., Harvard, C., Locker, R., Friedman, J.M., Langlois, S., Lewis, M.E.S., Van Allen, M., Somerville, M., Arbour, L., Clarke, L., McGilivray, B., Yong, S.L., Siegel-Bartel, J., Rajcan-Separovic, E.
Format:	Artikel
Sprache:	eng
Schlagworte:	11q12.3-13.1 7q36.3 array CGH Chromosome Aberrations Chromosome Disorders - genetics Chromosomes, Human, Pair 11 - genetics Chromosomes, Human, Pair 7 - genetics Chromosomes, Human, X - genetics de novo microdeletion and microduplication DNA Primers Female Humans In Situ Hybridization, Fluorescence intellectual disability Intellectual Disability - genetics Male Microsatellite Repeats - genetics Nucleic Acid Hybridization - genetics Oligonucleotide Array Sequence Analysis - methods Pedigree Polymerase Chain Reaction Xp22.3
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Beschreibung
Zusammenfassung:	Intellectual disability (ID) affects about 3% of the population (IQ
ISSN:	1552-4825 1552-4833
DOI:	10.1002/ajmg.a.31015