Non-random asynchronous replication at 22q11.2 favours unequal meiotic crossovers leading to the human 22q11.2 deletion.
about
Practical guidelines for managing patients with 22q11.2 deletion syndromeAnalysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplicationsA deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and reviewMolecular mechanisms and diagnosis of chromosome 22q11.2 rearrangementsDGCR6 at the proximal part of the DiGeorge critical region is involved in conotruncal heart defects.Signature MicroRNA expression patterns identified in humans with 22q11.2 deletion/DiGeorge syndromeMicrodeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA.Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndromeRefining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH.Cleft palate in a patient with the nested 22q11.2 LCR C to D deletion.
P2860
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P2860
Non-random asynchronous replication at 22q11.2 favours unequal meiotic crossovers leading to the human 22q11.2 deletion.
description
2004 nî lūn-bûn
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2004 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունիսին հրատարակված գիտական հոդված
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2004年の論文
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2004年論文
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2004年論文
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2004年論文
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2004年論文
@zh-mo
2004年論文
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2004年论文
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name
Non-random asynchronous replic ...... to the human 22q11.2 deletion.
@ast
Non-random asynchronous replic ...... to the human 22q11.2 deletion.
@en
type
label
Non-random asynchronous replic ...... to the human 22q11.2 deletion.
@ast
Non-random asynchronous replic ...... to the human 22q11.2 deletion.
@en
prefLabel
Non-random asynchronous replic ...... to the human 22q11.2 deletion.
@ast
Non-random asynchronous replic ...... to the human 22q11.2 deletion.
@en
P2860
P356
P1476
Non-random asynchronous replic ...... to the human 22q11.2 deletion
@en
P2093
P2860
P304
P356
10.1136/JMG.2003.016352
P407
P577
2004-06-01T00:00:00Z