Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients
about
Non-T cell activation linker (NTAL): a transmembrane adaptor protein involved in immunoreceptor signalingCharacterization and gene structure of a novel retinoblastoma-protein-associated protein similar to the transcription regulator TFII-ILow-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndromeWilliams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23A dual comparative approach: integrating lines of evidence from human evolutionary neuroanatomy and neurodevelopmental disordersVI. Genome structure and cognitive map of Williams syndrome.Williams-Beuren syndrome: an update and review for the primary physician.Williams (Williams Beuren) syndrome: a distinct neurobehavioral disorder.Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting.A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes.Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.Comparative mapping of the region of human chromosome 7 deleted in williams syndrome.Integration of hepatitis B virus DNA into chromosomal DNA during acute hepatitis BWilliams syndrome: an update on clinical and molecular aspects.Extracellular matrix and the mechanics of large artery development.Coexistence of supravalvular aortic stenosis and osteogenesis imperfectaEchocardiographic Characterization of Postnatal Development in Mice with Reduced Arterial Elasticity.Vascular extracellular matrix and arterial mechanics.Molecular mechanisms of OLIG2 transcription factor in brain cancer.Two generations of identical twins with ELN deletion.Injury prevention.Pentapeptide sharing between Corynebacterium diphtheria toxin and the human neural protein network.Mutation rate in human microsatellites.Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.Transitional implants in a patient with Williams-Beuren syndrome: a four-year follow-up.
P2860
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P2860
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients
description
1996 nî lūn-bûn
@nan
1996 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Identification of genes from a ...... in Williams syndrome patients
@ast
Identification of genes from a ...... in Williams syndrome patients
@en
Identification of genes from a ...... in Williams syndrome patients
@en-gb
Identification of genes from a ...... in Williams syndrome patients
@nl
type
label
Identification of genes from a ...... in Williams syndrome patients
@ast
Identification of genes from a ...... in Williams syndrome patients
@en
Identification of genes from a ...... in Williams syndrome patients
@en-gb
Identification of genes from a ...... in Williams syndrome patients
@nl
prefLabel
Identification of genes from a ...... in Williams syndrome patients
@ast
Identification of genes from a ...... in Williams syndrome patients
@en
Identification of genes from a ...... in Williams syndrome patients
@en-gb
Identification of genes from a ...... in Williams syndrome patients
@nl
P2093
P3181
P356
P1433
P1476
Identification of genes from a ...... in Williams syndrome patients
@en
P2093
D Martindale
J Brinkman
J Huizenga
L R Osborne
S W Scherer
P304
P3181
P356
10.1006/GENO.1996.0469
P407
P50
P577
1996-09-01T00:00:00Z