Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction
about
Genomic disorders on 22q11Breakpoint Associated with a novel 2.3 Mb deletion in the VCFS region of 22q11 and the role of Alu (SINE) in recurring microdeletionsChromosomal translocations and palindromic AT-rich repeatsCharacterization of the past and current duplication activities in the human 22q11.2 regionMeiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangementsPalindrome-mediated chromosomal translocations in humans.Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.Familial complex chromosome rearrangement ascertained by in situ hybridisation.From microscopes to microarrays: dissecting recurrent chromosomal rearrangements.The effect of translocation-induced nuclear reorganization on gene expression.Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.AT-rich palindromes mediate the constitutional t(11;22) translocation.Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) familiesA common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation.Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: an update and literature review.Paternal origin of the de novo constitutional t(11;22)(q23;q11).Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22)Comparative mapping of the constitutional and tumor-associated 11;22 translocations.AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12.Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.Predisposition for breast cancer in carriers of constitutional translocation 11q;22q.The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.Anesthesia in a patient with chromosome 11;22 translocation: a case report and literature review.Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.Nonhomologous chromatid exchange in hereditary and sporadic renal cell carcinomasComparison of constitutional and tumor-associated 11;22 translocations: nonidentical breakpoints on chromosomes 11 and 22Prenatal screening characteristics in Emanuel syndrome: a case series and review of the literature.Marker chromosomes.Pediatric peripheral neuroectodermal tumors, oncogenes, and differentiation.Human embryonic stem cells carrying an unbalanced translocation demonstrate impaired differentiation into trophoblasts: an in vitro model of human implantation failure.Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications.Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution.CD3G is within 200 kb of the leukemic t(4;11) translocation breakpoint.Congenital preauricular sinuses associated with dark hair coloration in one family.Genetic variation affects de novo translocation frequency.
P2860
Q24563977-AF90C44F-C40B-4243-8402-396CDD6C8A79Q25257898-CB69AE37-5950-4592-A2D1-8D86DF544CC7Q27024347-C3801103-DFFF-4933-B78C-3319BD202607Q28742657-2121AB59-C31A-4E2E-94CC-4BFA99991363Q30899679-B16FFBB8-D9B3-4984-83A4-927613A9F7E9Q33608623-6993ED9F-80B3-4257-91C6-61202C432AA8Q33608641-9449745E-A937-4D6D-AA16-940295054B99Q33668703-42118D23-4B34-48FB-B407-FB55896F4872Q33678031-F98729D0-BC5A-478D-A682-C11175A84CC4Q33678480-39904988-06EE-4A08-9DC8-2BE46F5D563FQ33805828-43F3F09E-F0AC-46E2-90DE-D38456D81995Q33812517-27FA81DC-3E89-48CE-93CE-23E028B154F3Q33904434-86E1D007-9BD1-4B99-B274-3B58404ACD1EQ34043814-4536CAB3-8FD9-47F1-B46D-9A4F944C9FC1Q34142712-D2274DB3-11E9-4BFD-ABA8-639F775051F0Q34146317-64FD0D98-FB66-4713-A3F3-5F997B6D2020Q34146321-A7E00EC1-6DD6-49A1-9367-FDA644545155Q34242739-10F06EE6-5B31-451A-975E-AFCB862F79D0Q34329295-BD6D00B5-AFA2-4767-97B5-A7484E3148ABQ34389097-013BD560-B099-4B3D-9C22-1D3F59ABAE74Q34452268-D064BAEE-F835-44A6-9A84-9AFDF0C6D160Q35015835-FB430FA2-B3F7-414B-87D6-A4E700AEDA35Q35197297-ABD0BD94-DA80-4782-8A16-30B2B8573FFAQ35698928-928A5BA6-E307-4313-B065-51162FAA20ECQ35749729-3926EDB6-86E1-4CBB-839F-099032113671Q35889351-A0FBC043-2950-4E12-A357-EC9E985F8461Q35913621-ADE62982-EF6D-4945-B034-2F0D68F4DF2DQ36292208-16A59F42-6045-4677-B973-D2EF9EC60F14Q37312490-273A89C9-D58D-4FAE-B6D8-8B75D6B2F91FQ37362243-265D4383-3123-4E4B-996C-92E9E66E10C5Q37395598-A4E3B460-2229-4947-8024-3D33CFB96843Q37995487-8D497D07-F72D-444D-AFE0-E267ED3F0499Q38010219-99862887-2462-4B22-AEFE-3A8E0032B196Q38037683-03F63282-B6A7-4BF9-AE26-63A4CF4938F9Q38940959-F202C5D9-AF4B-46A5-8EA8-696A52351A18Q39068495-0B0BD0E2-ED19-4F2A-AC42-1F711AB0B62CQ40830464-0F1F78B6-562F-40FA-91CC-1C231B9A4788Q41704783-24CE388F-BFE9-472A-A5B7-C5F0C291905EQ42047581-C34E5426-3104-45CB-85A6-654C8B62BDFFQ42150499-C3606E44-A7AA-41AD-8CC2-0A4CECBDB50C
P2860
Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction
description
1980 nî lūn-bûn
@nan
1980 թուականին հրատարակուած գիտական յօդուած
@hyw
1980 թվականին հրատարակված գիտական հոդված
@hy
1980年の論文
@ja
1980年論文
@yue
1980年論文
@zh-hant
1980年論文
@zh-hk
1980年論文
@zh-mo
1980年論文
@zh-tw
1980年论文
@wuu
name
Site-specific reciprocal trans ...... s with 3:1 meiotic disjunction
@ast
Site-specific reciprocal trans ...... s with 3:1 meiotic disjunction
@en
Site-specific reciprocal trans ...... s with 3:1 meiotic disjunction
@nl
type
label
Site-specific reciprocal trans ...... s with 3:1 meiotic disjunction
@ast
Site-specific reciprocal trans ...... s with 3:1 meiotic disjunction
@en
Site-specific reciprocal trans ...... s with 3:1 meiotic disjunction
@nl
prefLabel
Site-specific reciprocal trans ...... s with 3:1 meiotic disjunction
@ast
Site-specific reciprocal trans ...... s with 3:1 meiotic disjunction
@en
Site-specific reciprocal trans ...... s with 3:1 meiotic disjunction
@nl
P356
P1476
Site-specific reciprocal trans ...... s with 3:1 meiotic disjunction
@en
P2093
B S Emanuel
E H Zackai
P304
P356
10.1002/AJMG.1320070412
P407
P577
1980-01-01T00:00:00Z