Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams’ syndrome patients in Saudi Arabia

Journal article

Open access

Peer reviewed

Molecular cytogenetics, Vol.9(1), pp.65-65

12/08/2016

PMCID: PMC4981984

PMID: 27525043

Abstract

Array-CGH

Congenital heart defects

FISH

qPCR

Williams Syndrome

url

https://doi.org/10.1186/s13039-016-0266-4View

Published (Version of record) Open

1 Record Views

Title: Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams’ syndrome patients in Saudi Arabia
Creators - without role: I. R. Hussein - King Abdulaziz University
A. Magbooli - King Abdulaziz University
E. Huwait - King Abdulaziz University
A. Chaudhary - King Abdulaziz University
R. Bader - King Abdulaziz University
M. Gari - King Abdulaziz University
F. Ashgan - King Abdulaziz University
M. Alquaiti - King Abdulaziz University
A. Abuzenadah - King Abdulaziz University
M. AlQahtani - King Abdulaziz University
Publication Details: Molecular cytogenetics, Vol.9(1), pp.65-65
Publisher: BioMed Central
Grant note: P-L-11-0556 / ;
Identifiers: 9936986408331
Academic Unit: King Abdulaziz University
Language: English
Resource Type: Journal article