Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.
about
Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegansLow-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.Genomic disorders on 22q11Two functional copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locusA deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and reviewPhenotype of adults with the 22q11 deletion syndrome: A reviewSchizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation.Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.Protein components of the microRNA pathway and human diseases.Simultaneous, multilocus FISH analysis for detection of microdeletions in the diagnostic evaluation of developmental delay and mental retardation.How many breaks do we need to CATCH on 22q11?Schizophrenia and chromosomal deletions within 22q11.2.Goosecoid-like sequences and the smallest region of deletion overlap in DiGeorge and velocardiofacial syndromes.Linkage studies suggest a possible locus for bipolar disorder near the velo-cardio-facial syndrome region on chromosome 22.The organization of the gamma-glutamyl transferase genes and other low copy repeats in human chromosome 22q11.Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein.Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes.A common region of 10p deleted in DiGeorge and velocardiofacial syndromes
P2860
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P2860
Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Molecular cytogenetic characte ...... escence in situ hybridization.
@en
Molecular cytogenetic characte ...... escence in situ hybridization.
@nl
type
label
Molecular cytogenetic characte ...... escence in situ hybridization.
@en
Molecular cytogenetic characte ...... escence in situ hybridization.
@nl
prefLabel
Molecular cytogenetic characte ...... escence in situ hybridization.
@en
Molecular cytogenetic characte ...... escence in situ hybridization.
@nl
P2093
P356
P1433
P1476
Molecular cytogenetic characte ...... rescence in situ hybridization
@en
P2093
P304
P356
10.1006/GENO.1993.1339
P577
1993-08-01T00:00:00Z