Pages that link to "Q35199660"
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The following pages link to Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13 (Q35199660):
Displaying 50 items.
- Human collagen genes encoding basement membrane alpha 1 (IV) and alpha 2 (IV) chains map to the distal long arm of chromosome 13 (Q24295298) (← links)
- A novel POU homeodomain gene specifically expressed in cells of the developing mammalian nervous system (Q24629779) (← links)
- Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma (Q24630136) (← links)
- Deletion mapping of human chromosome 5 using chromosome-specific DNA probes (Q24675611) (← links)
- Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms (Q28256462) (← links)
- Assignment of human ferritin genes to chromosomes 11 and 19q13.3----19qter (Q28305793) (← links)
- Molecular genetic approach to human meningioma: loss of genes on chromosome 22 (Q30502412) (← links)
- A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes (Q32066752) (← links)
- Separation of anti-proliferation and anti-apoptotic functions of retinoblastoma protein through targeted mutations of its A/B domain (Q33267341) (← links)
- Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome (Q33325218) (← links)
- Construction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map. (Q33563058) (← links)
- High recombination between two physically close human basement membrane collagen genes at the distal end of chromosome 13q. (Q33567371) (← links)
- Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma (Q33592598) (← links)
- A linkage map of three anonymous human DNA fragments and SOD-1 on chromosome 21. (Q33931702) (← links)
- A chromosome 11-linked determinant controls fetal globin expression and the fetal-to-adult globin switch (Q34366910) (← links)
- Restriction fragment length polymorphism studies show consistent loss of chromosome 3p alleles in small cell lung cancer patients' tumors (Q34559345) (← links)
- Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred (Q34561886) (← links)
- Cosmid vectors for rapid genomic walking, restriction mapping, and gene transfer (Q34611719) (← links)
- Application of intragenic DNA probes in prenatal screening for retinoblastoma gene carriers in the United Kingdom. (Q35066308) (← links)
- Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions (Q35194344) (← links)
- Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies (Q35194870) (← links)
- Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene (Q35197191) (← links)
- Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome. (Q35198658) (← links)
- A primary genetic map of chromosome 13q. (Q35198742) (← links)
- Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13. (Q35199131) (← links)
- Etiological heterogeneity in X-linked spastic paraplegia (Q35199527) (← links)
- Isolation and regional mapping of DNA sequences unique to human chromosome 21. (Q35199586) (← links)
- Chromosome 13 homozygosity in osteosarcoma without retinoblastoma (Q35200618) (← links)
- Evidence for the close linkage between lymphocyte cytosol polypeptide with molecular weight of 64,000 (LCP1) and esterase D. (Q35200661) (← links)
- Regional mapping of six cloned DNA sequences on human chromosome 7. (Q35200793) (← links)
- Linkage of the Wilson disease gene to chromosome 13 in North-American pedigrees (Q35245651) (← links)
- Isolation and analysis of DNA markers specific to human chromosome 15. (Q35245692) (← links)
- Mapping of Alport syndrome to the long arm of the X chromosome (Q35246146) (← links)
- Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome. (Q35247684) (← links)
- Eight closely linked loci place the Wilson disease locus within 13q14-q21. (Q35247717) (← links)
- Fine structure DNA mapping studies of the chromosomal region harboring the genetic defect in neurofibromatosis type I. (Q35550484) (← links)
- Construction of a map of the short arm of human chromosome 6 (Q35608703) (← links)
- Genomic imprinting of the human serotonin-receptor (HTR2) gene involved in development of retinoblastoma (Q35882156) (← links)
- A straightforward approach to isolate DNA sequences with potential linkage to the retinoblastoma locus (Q36414839) (← links)
- Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy (Q36423501) (← links)
- The single copy gene coding for human alpha 1 (IV) procollagen is located at the terminal end of the long arm of chromosome 13. (Q36480098) (← links)
- Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas (Q37401663) (← links)
- Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition (Q37542430) (← links)
- Correlation between retinoblastoma gene expression and differentiation in human testicular tumors (Q37559305) (← links)
- Loss of polymorphic restriction fragments in malignant melanoma: implications for tumor heterogeneity (Q37679541) (← links)
- Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus (Q37680904) (← links)
- Suppression of tumor-forming ability and related traits in MCF-7 human breast cancer cells by fusion with immortal mammary epithelial cells (Q37722844) (← links)
- An appraisal of the application of recombinant DNA techniques to chromosome defects (Q39816011) (← links)
- PstI RFLP for the anonymous [D13S2] (p9D11) probe. (Q40448065) (← links)
- Inverted duplication of JH associated with chromosome 14 translocation and T-cell leukemia in ataxia-telangiectasia (Q40597117) (← links)