about
The sequence of human chromosome 21 and implications for research into Down syndromeMutational analyses of the signals involved in the subcellular location of DSCR1.Aneuploidy: cancer's fatal flaw?Human aneuploidy: mechanisms and new insights into an age-old problemRecombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16Overexpression of FABP7 in Down syndrome fetal brains is associated with PKNOX1 gene-dosage imbalanceClinical aspects, prenatal diagnosis, and pathogenesis of trisomy 16 mosaicismUniparental disomy as a mechanism for human genetic diseaseIdentification and characterization of SA/Scc3p subunits in the Xenopus and human cohesin complexesA link between high serum levels of human chorionic gonadotrophin and chorionic expression of its mature functional receptor (LHCGR) in Down's syndrome pregnanciesIdentification of aneuploidy-tolerating mutationsMouse HFM1/Mer3 is required for crossover formation and complete synapsis of homologous chromosomes during meiosisGenome-wide maps of recombination and chromosome segregation in human oocytes and embryos show selection for maternal recombination ratesMultipoint genetic mapping with uniparental disomy dataMultipoint genetic mapping with trisomy data.Detection of structural and numerical chromosome abnormalities in interphase cells using spectral imaging.Spectral imaging in preconception/preimplantation genetic diagnosis of aneuploidy: multicolor, multichromosome screening of single cells.A calcineurin inhibitory protein overexpressed in Down's syndrome interacts with the product of a ubiquitously expressed transcript.Tonguing behaviours in persons with Down syndrome: moderator of the effects of negative mood on behaviour problems.Meiotic recombination in human oocytes.Night Monkey Hybrids Exhibit De Novo Genomic and Karyotypic Alterations: The First Such Case in PrimatesNon-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach.Duplication of 16q22-->qter confirmed by fluorescence in situ hybridisation and molecular analysisMolecular studies of non-disjunction in trisomy 16.Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome.High resolution gene mapping of the human alpha globin locusDown syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH.Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology?Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21.Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7Maternal non-Mendelian inheritance of a reduced lifespan? A hypothesis.A macaque model for studying mechanisms controlling oocyte development and maturation in human and non-human primates.Down syndrome: genetic recombination and the origin of the extra chromosome 21.Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line.The origin of abnormalities in recurrent aneuploidy/polyploidyPostoperative adverse outcomes in intellectually disabled surgical patients: a nationwide population-based studyPolymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome.Single cell sequencing reveals low levels of aneuploidy across mammalian tissues.Synaptonemal complex components persist at centromeres and are required for homologous centromere pairing in mouse spermatocytes.Sex differences in the cholinergic basal forebrain in the Ts65Dn mouse model of Down syndrome and Alzheimer's disease.
P2860
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P2860
description
1984 nî lūn-bûn
@nan
1984 թուականին հրատարակուած գիտական յօդուած
@hyw
1984 թվականին հրատարակված գիտական հոդված
@hy
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
name
Trisomy in man
@ast
Trisomy in man
@en
Trisomy in man
@nl
type
label
Trisomy in man
@ast
Trisomy in man
@en
Trisomy in man
@nl
prefLabel
Trisomy in man
@ast
Trisomy in man
@en
Trisomy in man
@nl
P1476
Trisomy in man
@en
P2093
P A Jacobs
T J Hassold
P356
10.1146/ANNUREV.GE.18.120184.000441
P407
P577
1984-01-01T00:00:00Z