Pages that link to "Q35673611"
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The following pages link to Isolation and characterization of a major tandem repeat family from the human X chromosome (Q35673611):
Displaying 50 items.
- Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes (Q24298720) (← links)
- Localization of two human homologs, HHR6A and HHR6B, of the yeast DNA repair gene RAD6 to chromosomes Xq24-q25 and 5q23-q31 (Q24321697) (← links)
- Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase (Q24568191) (← links)
- Structure and distribution of an Alu-type deletion mutation in Sandhoff disease (Q24618126) (← links)
- Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism (Q24679266) (← links)
- Nucleotide sequences of Dictyostelium discoideum developmentally regulated cDNAs rich in (AAC) imply proteins that contain clusters of asparagine, glutamine, or threonine. (Q30469450) (← links)
- Evidence for a fast, intrachromosomal conversion mechanism from mapping of nucleotide variants within a homogeneous alpha-satellite DNA array (Q30872875) (← links)
- In situ hybridization to cytogenetic bands of yeast artificial chromosomes covering 50% of human Xq24-Xq28 DNA (Q30883181) (← links)
- JKT-1 is not a human seminoma cell line (Q33294472) (← links)
- Molecular cloning and analysis of the fragile X region in man (Q33563651) (← links)
- Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting (Q33596140) (← links)
- The human Y chromosome (Q33672139) (← links)
- Sex chromosome aneuploidies in sperm of 47,XYY men. (Q33710111) (← links)
- Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA. (Q34047384) (← links)
- A 47,XXY female with unusual genitalia (Q34296451) (← links)
- DNMT3B mutations and DNA methylation defect define two types of ICF syndrome. (Q34373710) (← links)
- Human Xq24-Xq28: approaches to mapping with yeast artificial chromosomes (Q34403036) (← links)
- Bioinformatics tools allow targeted selection of chromosome enumeration probes and aneuploidy detection (Q34498064) (← links)
- Cloning and characterization of a dispersed, multicopy, X chromosome sequence in Drosophila melanogaster (Q34618654) (← links)
- Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes (Q34708825) (← links)
- Hematopoiesis-restricted minor histocompatibility antigens HA-1- or HA-2-specific T cells can induce complete remissions of relapsed leukemia (Q34808353) (← links)
- Paternal heterochromatin formation in human embryos is H3K9/HP1 directed and primed by sperm-derived histone modifications. (Q34833234) (← links)
- A Cys138-to-Arg substitution in the GM2 activator protein is associated with the AB variant form of GM2 gangliosidosis (Q35195467) (← links)
- Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect (Q35197526) (← links)
- Characterization of human centromeric regions of specific chromosomes by means of alphoid DNA sequences (Q35199174) (← links)
- Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation (Q35200300) (← links)
- Construction and analysis of DNA sequence libraries from flow-sorted chromosomes: practical and theoretical considerations (Q35279780) (← links)
- Sex chromosome loss and aging: in situ hybridization studies on human interphase nuclei (Q35643922) (← links)
- Interphase cytogenetic analysis of cervical intraepithelial neoplasia (Q35763779) (← links)
- X inactivation in human testicular tumors. XIST expression and androgen receptor methylation status (Q35763875) (← links)
- Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays (Q35804293) (← links)
- New rapid test for prenatal detection of trisomy 21 (Down's syndrome): preliminary report (Q35822192) (← links)
- Near-haploidy and subsequent polyploidization characterize the progression of peripheral chondrosarcoma. (Q35829605) (← links)
- X chromosome inactivation of the human TIMP gene. (Q35851082) (← links)
- A survey of the genomic distribution of alpha satellite DNA on all the human chromosomes, and derivation of a new consensus sequence (Q35917829) (← links)
- PCR amplification of tandemly repeated DNA: analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA (Q35935165) (← links)
- Homologous alpha satellite sequences on human acrocentric chromosomes with selectivity for chromosomes 13, 14 and 21: implications for recombination between nonhomologues and Robertsonian translocations. (Q35997271) (← links)
- Translocation and amplification of an X-chromosome DNA repeat in inbred strains of mice (Q36128888) (← links)
- Human Artificial Chromosomes with Alpha Satellite-Based De Novo Centromeres Show Increased Frequency of Nondisjunction and Anaphase Lag (Q36138989) (← links)
- Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome (Q36139991) (← links)
- Human Extravillous Trophoblasts Penetrate Decidual Veins and Lymphatics before Remodeling Spiral Arteries during Early Pregnancy (Q36247914) (← links)
- FISH analysis of six chromosomes in unfertilized human oocytes after polar body removal (Q36269448) (← links)
- Repeated DNA sequences in the distal long arm of the human X chromosome (Q36425673) (← links)
- Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis (Q36473258) (← links)
- Isolation and characterization of an alpha-satellite repeated sequence from human chromosome 22. (Q36479991) (← links)
- The organization of two related subfamilies of a human tandemly repeated DNA is chromosome specific (Q36496918) (← links)
- Chromosome specific DNA hybridization in suspension for flow cytometric detection of chimerism in bone marrow transplantation and leukemia (Q36709543) (← links)
- Replication timing of DNA sequences associated with human centromeres and telomeres (Q36774402) (← links)
- Duplication of the short arm of the X chromosome in mother and daughter (Q36783772) (← links)
- Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin (Q36824341) (← links)