Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome).
about
Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.Runs of homozygosity associated with speech delay in autism in a taiwanese han population: evidence for the recessive model.Jacobsen Syndrome: Surgical Complications due to Unsuspected Diagnosis, the Importance of Molecular Studies in Patients with Craniosynostosis.The use of array-CGH in a cohort of Greek children with developmental delay.
P2860
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome).
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Detailed molecular and clinica ...... mosome 11 (Jacobsen syndrome).
@ast
Detailed molecular and clinica ...... mosome 11 (Jacobsen syndrome).
@en
type
label
Detailed molecular and clinica ...... mosome 11 (Jacobsen syndrome).
@ast
Detailed molecular and clinica ...... mosome 11 (Jacobsen syndrome).
@en
prefLabel
Detailed molecular and clinica ...... mosome 11 (Jacobsen syndrome).
@ast
Detailed molecular and clinica ...... mosome 11 (Jacobsen syndrome).
@en
P2093
P2860
P356
P1476
Detailed molecular and clinica ...... mosome 11 (Jacobsen syndrome).
@en
P2093
Aikaterini Metaxotou
Eirini Louizou
Emmanouil Manolakos
George Kitsos
Ioannis Papoulidis
Konstantinos Kefalas
Loretta Thomaidis
Michael B Petersen
Panagiota Tsoplou
Panagiotis Peitsidis
P2860
P2888
P356
10.1186/1755-8166-2-26
P50
P577
2009-12-09T00:00:00Z
P5875
P6179
1049612985