Pages that link to "Q40166062"

The following pages link to Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques (Q40166062):

Displaying 50 items.

• Deletion mapping of human chromosome 5 using chromosome-specific DNA probes (Q24675611) (← links)
• The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP (Q29040598) (← links)
• A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes (Q32066752) (← links)
• The human genes for complement components 6 (C6) and 9 (C9) are closely linked on chromosome 5. (Q33593510) (← links)
• The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3. (Q33931052) (← links)
• Extensive DNA sequence homologies between the human Y and the long arm of the X chromosome (Q33931501) (← links)
• Mapping of the mouse X chromosome using random genomic probes and an interspecific mouse cross (Q33932173) (← links)
• Origin of leukemic relapse after bone marrow transplantation detected by restriction fragment length polymorphism (Q34522782) (← links)
• Molecular studies of trisomy 18 (Q35194706) (← links)
• Segregation of all four major fibrillar collagen genes in the Marfan syndrome. (Q35199604) (← links)
• The parental origin of X chromosomes in XX males determined using restriction fragment length polymorphisms (Q35199871) (← links)
• A strategy to reveal high-frequency RFLPs along the human X chromosome (Q35199942) (← links)
• Genetic distances between the Utah Mormons and related populations (Q35199964) (← links)
• The use of multiple restriction fragment length polymorphisms in prenatal risk estimation. I. X-linked diseases. (Q35200161) (← links)
• Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21. (Q35200319) (← links)
• Molecular heterogeneity in the mild autosomal dominant forms of osteogenesis imperfecta (Q35200439) (← links)
• Isolation and subregional mapping of an arbitrary cloned probe detecting a common RFLP on human chromosome 2. (Q35200570) (← links)
• Chromosome 13 homozygosity in osteosarcoma without retinoblastoma (Q35200618) (← links)
• Use of molecular haplotypes specific for the human pro alpha 2(I) collagen gene in linkage analysis of the mild autosomal dominant forms of osteogenesis imperfecta (Q35200775) (← links)
• A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37 (Q35200781) (← links)
• The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1. (Q35200834) (← links)
• Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19. (Q35200843) (← links)
• A DNA probe detecting multiple haplotypes of the human Y chromosome (Q35200865) (← links)
• A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm. (Q35280432) (← links)
• Human dihydrofolate reductase gene is located in chromosome 5 and is unlinked to the related pseudogenes (Q36251997) (← links)
• A highly polymorphic locus in human DNA revealed by cosmid-derived probes (Q36423825) (← links)
• Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome (Q36424466) (← links)
• Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to human chromosome 12q. (Q36424470) (← links)
• Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26?qter (Q36587135) (← links)
• Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition (Q37542430) (← links)
• Polymorphisms of a human variable heavy chain gene show linkage with constant heavy chain genes (Q37580444) (← links)
• Loss of polymorphic restriction fragments in malignant melanoma: implications for tumor heterogeneity (Q37679541) (← links)
• The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency (Q37686181) (← links)
• The role of somatic cell genetics in human gene mapping (Q39745653) (← links)
• Optimizing selection of restriction enzyme in the search for ONA variants (Q40463279) (← links)
• A locus on chromosome 11p with multiple restriction site polymorphisms (Q40612948) (← links)
• Retinoblastoma: a model of oncogenesis (Q41575472) (← links)
• Construction of linkage maps with DNA markers for human chromosomes. (Q43486574) (← links)
• Molecular nature of chromosome 5q loss in colorectal tumors and desmoids from patients with familial adenomatous polyposis (Q43737604) (← links)
• Search for putative suppressor genes in meningioma: significance of chromosome 22 (Q44326870) (← links)
• Ehlers-Danlos syndrome type IV: cosegregation of the phenotype to a COL3A1 allele of type III procollagen (Q57197861) (← links)
• Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism (Q59053447) (← links)
• Loss of genes on the short arm of chromosome 11 in bladder cancer (Q59066203) (← links)
• DNA polymorphism in the 5' flanking region of the human carbonic anhydrase II gene on chromosome 8 (Q70082966) (← links)
• Confirmation of the close linkage between the loci for human apolipoproteins AI and AIV by the use of a cloned cDNA probe and two restriction site polymorphisms (Q70122716) (← links)
• Restriction fragment length polymorphisms in the D7S1 region of human chromosome 7 (Q70122724) (← links)
• Regional assignments of three polymorphic DNA segments on human chromosome 15 (Q70146102) (← links)
• Interpretation of LOD scores with a set of marker loci (Q70979083) (← links)
• The locus for apolipoprotein CII is closely linked to the apolipoprotein E locus on chromosome 19 in man (Q72389673) (← links)
• Mapping X-linked ophthalmic diseases. Provisional assignment of the locus for choroideremia to Xq13-q24 (Q93599158) (← links)