| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1991PNAS...88.6157N |
| P356 | DOI | 10.1073/PNAS.88.14.6157 |
| P932 | PMC publication ID | 52041 |
| P698 | PubMed publication ID | 2068096 |
| P5875 | ResearchGate publication ID | 21088126 |
| P2093 | author name string | Caskey CT | |
| Ballabio A | |||
| Nelson DL | |||
| Gibbs RA | |||
| Chinault AC | |||
| Pieretti M | |||
| Bies RD | |||
| Maley JA | |||
| Victoria MF | |||
| Webster TD | |||
| P2860 | cites work | Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 |
| Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase | Q26778389 | ||
| A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity | Q26778490 | ||
| Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresis | Q28267117 | ||
| Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome | Q28273791 | ||
| Yeast artificial chromosomes with 200- to 800-kilobase inserts of human DNA containing HLA, V kappa, 5S, and Xq24-Xq28 sequences. | Q33840781 | ||
| Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA. | Q33843918 | ||
| A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones | Q33912732 | ||
| Rapid screening of a human genomic library in yeast artificial chromosomes for single-copy sequences | Q34294624 | ||
| Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources | Q34301388 | ||
| Use of yeast artificial chromosome clones for mapping and walking within human chromosome segment 18q21.3. | Q34307736 | ||
| Construction of human chromosome 21-specific yeast artificial chromosomes | Q34326220 | ||
| Human Xq24-Xq28: approaches to mapping with yeast artificial chromosomes | Q34403036 | ||
| Isolation of single-copy human genes from a library of yeast artificial chromosome clones | Q34450414 | ||
| Five polymorphic microsatellite VNTRs on the human X chromosome. | Q34481619 | ||
| Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction | Q34993293 | ||
| Mapping the Drosophila genome with yeast artificial chromosomes | Q35221352 | ||
| Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment | Q35245521 | ||
| Isolation and localization of DNA segments from specific human chromosomes | Q36389671 | ||
| A rodent-human hybrid containing Xq24-qter translocated to a hamster chromosome expresses the Xq27 folate-sensitive fragile site | Q36418655 | ||
| A highly polymorphic locus in human DNA revealed by cosmid-derived probes | Q36423825 | ||
| Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors | Q36426834 | ||
| Genome linking with yeast artificial chromosomes | Q36427623 | ||
| Expression of the fragile (X) chromosome in an interspecific somatic cell hybrid | Q43445313 | ||
| A common language for physical mapping of the human genome | Q46940837 | ||
| Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives | Q52107660 | ||
| Cloning of human telomeres by complementation in yeast | Q58995576 | ||
| Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and Yq | Q60641507 | ||
| Transformation of yeast spheroplasts without cell fusion | Q68192987 | ||
| Electrophoretic separations of large DNA molecules by periodic inversion of the electric field | Q70022520 | ||
| P433 | issue | 14 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 6157-6161 | |
| P577 | publication date | 1991-07-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus | |
| P478 | volume | 88 |
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| Q28139171 | An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y |
| Q24629985 | Cloning of human and bovine homologs of SNF2/SWI2: a global activator of transcription in yeast S. cerevisiae |
| Q35643289 | Deletion and translocation of chromosome 11q13 sequences in cervical carcinoma cell lines. |
| Q42951290 | Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26. |
| Q46702230 | Fluorescent in-situ hybridization of cattle and sheep chromosomes with cloned human fragile-X DNA. |
| Q35024299 | High-resolution landmark framework for the sequence-ready mapping of Xq23-q26.1. |
| Q48081485 | Highly homologous loci on the X and Y chromosomes are hot-spots for ectopic recombinations leading to XX maleness. |
| Q72452811 | Impact of the human genome project on medical practice |
| Q33205256 | Isolation of cDNA sequences around the chromosomal breakpoint in a female with Lowe syndrome by direct screening of cDNA libraries with yeast artificial chromosomes |
| Q33223604 | Long-range walking techniques in positional cloning strategies |
| Q35195332 | Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly |
| Q36783665 | Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy. |
| Q77226444 | PCR based targeted genomic and cDNA differential display |
| Q28275781 | Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions |
| Q37144835 | Sequence-tagged site (STS) content mapping of human chromosomes: theoretical considerations and early experiences |
| Q33230917 | Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p |
| Q24336782 | The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase |
| Q48074603 | YAC contigs mapping the human COL4A5 and COL4A6 genes and DXS118 within Xq21.3–q22 |
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