Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction.
about
A contiguous Not I restriction map of band q22.3 of human chromosome 21Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13.3Molecular genetic approach to human meningioma: loss of genes on chromosome 22Long-distance restriction mapping of the proximal long arm of human chromosome 21 with Not I linking clones.Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17Molecular genetics of human chromosome 21.Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions.Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndromeA chromosome 11-linked determinant controls fetal globin expression and the fetal-to-adult globin switchDinucleotide repeat polymorphism at the D21S16 [correction of D1S16] locus.Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis.Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome.No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21.The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.Isolation and regional mapping of DNA sequences unique to human chromosome 21.Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomesTrisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.The probability of detecting the origin of nondisjunction of autosomal trisomiesMolecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 regionMinute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region.An hypervariable polymorphism detected in the human inter-alpha-trypsin inhibitor heavy chain gene ITIH2A high frequency EcoRI RFLP detected at the D21S13 locus.Chromosomal localization of glutamate receptor genes: relationship to familial amyotrophic lateral sclerosis and other neurological disorders of mice and humans.RFLPS at the D21S19 locus of human chromosome 21.Identification of polymorphisms by genomic denaturing gradient gel electrophoresis: application to the proximal region of human chromosome 21.Discerning non-disjunction in Down syndrome patients by means of GluK1-(AGAT)(n) and D21S2055-(GATA)(n) microsatellites on chromosome 21.Fluorescence microsatellite analysis to study the parental origin of the supernumerary chromosome in Down's syndrome.
P2860
Q24562094-EB76C32D-2B55-4459-8A3D-ED9DC280DF9AQ28237313-0E384A9A-D7C8-470D-BC37-32F62C9CCEDBQ30502412-71AD5AAB-88C9-420D-BB81-C9D53ADC1777Q31162099-CADDD3F1-7082-4D6D-93D1-3C3C349DE105Q33640527-418C36D2-1BDF-47A1-956C-C770D7E219A7Q33674852-66F24421-A013-43A1-8438-FF4495C1CB2FQ33916503-B5755EF0-1DA8-43D4-94DD-0A63AB6262DDQ34294835-5CDFFA8C-D183-4698-8A55-4C70F425013CQ34366910-683E863F-6FFA-4DB1-801B-6511F955ACEBQ35062770-D908A8B3-6D2A-4B15-8F9B-9388060DE754Q35195088-6104E06D-3853-4323-B6BB-B87860D4F85FQ35195816-1E374891-F585-419D-907B-FA95A5321CBAQ35195831-1F6F1692-FCB4-4986-A337-D9219AAFE39AQ35196333-0F886BD0-7899-4D84-83B1-5AD2C4495A17Q35197932-DD6AA49E-08A4-44A9-918C-9EA83FD8DAD8Q35199335-2E6FDF98-381C-43B0-B907-172BF9249499Q35199586-1A15B2EE-3F8B-44B9-98DB-1F6DB1A8E5A0Q35245989-13885B16-11EA-4414-9603-BE33F2515EA9Q35246004-5B6A94A1-4DEE-4DAA-9943-EFA3949E75D6Q35248326-D148FB68-AC49-4510-8A4F-D524DF14F313Q35643522-9CF7E6EF-254E-421A-8C29-55AE8F340399Q35643563-81E87D97-0703-4209-ADED-8C1B7A39A9A6Q35833422-2B0DB8C1-0448-4E6A-A99A-D8A8E2F50347Q35833434-908A2622-F018-41FD-A1B2-7975687E51EFQ36216333-36FBB9E8-257C-48C5-905E-8038BBAD17A6Q40472079-40F2A8F5-35DF-4A6D-8BFA-2D27348EBF9FQ40532514-7B941132-E149-4414-8A70-0EC7AF65C472Q41434138-4482F79C-8CE6-45EB-BED4-A97B0B86F1F4Q51993229-306FF761-43C2-468A-9343-903D7C39930D
P2860
Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction.
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
1985年论文
@zh
1985年论文
@zh-cn
name
Cloned DNA probes regionally m ...... the origin of nondisjunction.
@ast
Cloned DNA probes regionally m ...... the origin of nondisjunction.
@en
type
label
Cloned DNA probes regionally m ...... the origin of nondisjunction.
@ast
Cloned DNA probes regionally m ...... the origin of nondisjunction.
@en
prefLabel
Cloned DNA probes regionally m ...... the origin of nondisjunction.
@ast
Cloned DNA probes regionally m ...... the origin of nondisjunction.
@en
P2093
P2860
P356
P1476
Cloned DNA probes regionally m ...... the origin of nondisjunction.
@en
P2093
Ferguson-Smith MA
Stewart GD
P2860
P304
P356
10.1093/NAR/13.11.4125
P407
P577
1985-06-01T00:00:00Z