Pages that link to "Q34146317"

The following pages link to Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families (Q34146317):

Displaying 34 items.

• Genomic disorders on 22q11 (Q24563977) (← links)
• Small supernumerary marker chromosomes and their correlation with specific syndromes (Q26795731) (← links)
• Chromosomal translocations and palindromic AT-rich repeats (Q27024347) (← links)
• Chromosomal microdeletions: dissecting del22q11 syndrome (Q28206335) (← links)
• Meiotic 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. (Q30899679) (← links)
• 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 (Q33608623) (← links)
• MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q (Q33622853) (← links)
• A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2 (Q33638175) (← links)
• Palindrome-mediated chromosomal translocations in humans (Q33668703) (← links)
• The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats (Q33904580) (← links)
• AT-rich palindromes mediate the constitutional t(11;22) translocation. (Q34043814) (← links)
• Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22). (Q34142712) (← links)
• Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: an update and literature review (Q34242739) (← links)
• Segmental duplications: an 'expanding' role in genomic instability and disease (Q34389505) (← links)
• Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes (Q34452268) (← links)
• Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22) (Q35015835) (← links)
• Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats (Q35749729) (← links)
• The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements. (Q35913621) (← links)
• Anesthesia in a patient with chromosome 11;22 translocation: a case report and literature review (Q36292208) (← links)
• Derivative 11;22 (emanuel) syndrome: a case report and a review (Q36837814) (← links)
• Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region (Q37406676) (← links)
• Marker chromosomes (Q38010219) (← links)
• Molecular cloning of a translocation breakpoint hotspot in 22q11. (Q42907947) (← links)
• High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11). (Q48469722) (← links)
• Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH. (Q51905129) (← links)
• Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individuals. (Q51930316) (← links)
• Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males (Q74592036) (← links)
• Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11) (Q78513387) (← links)
• XX male with sex reversal and a de novo 11;22 translocation (Q80072646) (← links)
• Characterization of a cryptic 3.3 Mb deletion in a patient with a "balanced t(15;22) translocation" using high density oligo array CGH and gene expression arrays (Q80510578) (← links)
• Preferential alternate segregation in the common t(11;22)(q23;q11) reciprocal translocation: sperm FISH analysis in two brothers (Q81318818) (← links)
• FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22) (Q81498890) (← links)
• Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays (Q83163623) (← links)
• Whole Genome Low-Coverage Sequencing Concurrently Detecting Copy Number Variations and Their Underlying Complex Chromosomal Rearrangements by Systematic Breakpoint Mapping in Intellectual Deficiency/Developmental Delay Patients (Q98177815) (← links)