A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).
about
Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated toolsNon-B DB: a database of predicted non-B DNA-forming motifs in mammalian genomesPalindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal RearrangementsSmall supernumerary marker chromosomes and their correlation with specific syndromesChromosomal translocations and palindromic AT-rich repeatsChimeric negative regulation of p14ARF and TBX1 by a t(9;22) translocation associated with melanoma, deafness, and DNA repair deficiencyAnalysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation.Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations.Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints.Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation.X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3Genome-wide screen reveals replication pathway for quasi-palindrome fragility dependent on homologous recombination.On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease.DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation.A recurrent translocation is mediated by homologous recombination between HERV-H elements.Searching for non-B DNA-forming motifs using nBMST (non-B DNA motif search tool)Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs.One pedigree we all may have come from - did Adam and Eve have the chromosome 2 fusion?Complex small supernumerary marker chromosomes - an updateA New Case of a Complex Small Supernumerary Marker Chromosome: A Der(9)t(7;9)(p22;q22) due to a Maternal Balanced Rearrangement.Palindrome-mediated and replication-dependent pathogenic structural rearrangements within the NF1 gene.Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes.Constitutional t(8;22)(q24;q11.2) that mimics the variant Burkitt-type translocation in Philadelphia chromosome-positive chronic myeloid leukemia.
P2860
Q24595019-3296DA80-0F05-4BFA-B68D-A0F0B0CEBD97Q24611196-4E22EE75-52A2-4FA7-85FA-2A808EA2468DQ26741394-E59DCFC1-8D61-44ED-B34C-FCB1DD1C1582Q26795731-17C1E2F9-4BD5-4009-B55B-B29E644455F3Q27024347-DAA6AD30-1438-447E-A40A-AF867C706B0DQ28290365-2FC144E5-7509-4323-9FD3-EC7F2533BEE8Q33915581-D145C928-EFB2-4C80-90BB-9BA6F50EA070Q34332380-771BDF51-1911-43A0-98B6-2A78AFB08E51Q34452268-78FC0860-6FDF-4AD4-AFDE-7E7971EB2BA8Q34501235-4FB810A9-F3AE-4B06-A29C-A44C10D5133DQ34631531-C7D7733C-A4E7-4D13-B9EB-1DD6D6D341A5Q35039915-C6EB4912-8EE8-4C4D-B864-CFF36782B6D3Q35067254-96A98333-B4BA-4CFB-B103-E0A85312CAD2Q35226155-F11BE36A-6195-45C3-9489-DB1D268524FAQ35398079-00B23769-298D-4232-A223-8208A34BE403Q35799446-B207E921-246B-4FA3-ABF4-FF498A90A2C2Q35954644-6EBEF69C-62ED-4EAD-9CA6-61CA786DF2D4Q36666968-E7077D5C-F1A8-459E-AF37-D218A6CF9680Q37286048-BD4127EC-A448-4E5F-8750-F1CBBACE6758Q41911501-F5EFE5CA-DAC8-4146-9F1F-B82F51977DB2Q42723139-F103C7C3-FA4D-45E7-BD71-4A426DF707C3Q44108282-968BE3DB-47EE-445B-ACF5-A527B8352217Q48247965-85761701-7FF4-475B-926A-12175E39F0F0Q52675422-3BF0CB0D-6625-4F23-9354-C4B3790E3CAE
P2860
A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).
description
2010 nî lūn-bûn
@nan
2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t
@nl
A palindrome-mediated recurren ...... n: the t(8;22)(q24.13;q11.21).
@ast
A palindrome-mediated recurren ...... n: the t(8;22)(q24.13;q11.21).
@en
type
label
A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t
@nl
A palindrome-mediated recurren ...... n: the t(8;22)(q24.13;q11.21).
@ast
A palindrome-mediated recurren ...... n: the t(8;22)(q24.13;q11.21).
@en
prefLabel
A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t
@nl
A palindrome-mediated recurren ...... n: the t(8;22)(q24.13;q11.21).
@ast
A palindrome-mediated recurren ...... n: the t(8;22)(q24.13;q11.21).
@en
P2093
P2860
P1476
A palindrome-mediated recurren ...... n: the t(8;22)(q24.13;q11.21).
@en
P2093
April M Hacker
Beverly S Emanuel
Chad Haldeman-Englert
David Tomkins
Elaine H Zackai
G Reza Jalali
Georgio Gimelli
Harry A Drabkin
Hiroki Kurahashi
Jeff M Milunsky
P2860
P304
P356
10.1016/J.AJHG.2010.07.002
P407
P577
2010-07-30T00:00:00Z