Pages that link to "Q36423825"
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The following pages link to A highly polymorphic locus in human DNA revealed by cosmid-derived probes (Q36423825):
Displaying 50 items.
- Isolation of a candidate gene for choroideremia (Q24562765) (← links)
- An insertion deletion polymorphism associated with C-FES (Q24630523) (← links)
- Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium (Q24670212) (← links)
- Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases (Q24676605) (← links)
- An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry (Q24678018) (← links)
- Cloning of the T gene required in mesoderm formation in the mouse (Q28236865) (← links)
- Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13.3 (Q28237313) (← links)
- Exclusion of a schizophrenia susceptibility gene from the chromosome 5q11-q13 region: new data and a reanalysis of previous reports (Q30660558) (← links)
- Saturating the region of the polycystic kidney disease gene with NotI linking clones (Q30883220) (← links)
- Hybridization fingerprinting of high-density cDNA-library arrays with cDNA pools derived from whole tissues (Q33193212) (← links)
- Isolation of cDNA sequences around the chromosomal breakpoint in a female with Lowe syndrome by direct screening of cDNA libraries with yeast artificial chromosomes (Q33205256) (← links)
- Molecular analysis of human chromosome 16 cosmid clones containing NotI sites (Q33223603) (← links)
- Cloning the ends of size selected Sfi I fragments (Q33319362) (← links)
- Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter (Q33493313) (← links)
- Derivation of clones from the choroideremia locus by preparative field inversion gel electrophoresis (Q33494932) (← links)
- Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects (Q33595838) (← links)
- Linkage analysis in Marfan syndrome (Q33597166) (← links)
- Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1. (Q33598290) (← links)
- 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 (Q33648165) (← links)
- Detection of de novo mutations and analysis of their origin in families with X linked hypohidrotic ectodermal dysplasia (Q33673841) (← links)
- Genetic linkage map of 46 DNA markers on human chromosome 16. (Q33715735) (← links)
- Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region (Q34287832) (← links)
- Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia (Q34307943) (← links)
- Genetic linkage map of human chromosome 7 with 63 DNA markers (Q34365588) (← links)
- A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene (Q34460557) (← links)
- The pseudoautosomal boundary in man is defined by an Alu repeat sequence inserted on the Y chromosome (Q34561071) (← links)
- Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment. (Q35194286) (← links)
- A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11. (Q35195482) (← links)
- Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COL1A2 locus (Q35196278) (← links)
- Possible linkage of the estrogen receptor gene to breast cancer in a family with late-onset disease (Q35196668) (← links)
- Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization (Q35196840) (← links)
- Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome Ip36. (Q35197797) (← links)
- Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q. (Q35198651) (← links)
- A deductive method of haplotype analysis in pedigrees (Q35199197) (← links)
- Isolation and regional mapping of DNA sequences unique to human chromosome 21. (Q35199586) (← links)
- A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37 (Q35200781) (← links)
- Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19. (Q35200843) (← links)
- Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment (Q35245521) (← links)
- Chromosomal localization of the human proenkephalin and prodynorphin genes (Q35246049) (← links)
- Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families (Q35246067) (← links)
- Identification of more than 500 RFLPs by screening random genomic clones (Q35246565) (← links)
- New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization. (Q35247023) (← links)
- Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq (Q35247517) (← links)
- Identification and characterization of 23 RFLP loci by screening random cosmid genomic clones. (Q35555004) (← links)
- Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome (Q35611528) (← links)
- CRI-J177 (DYS152): a polymorphic Y chromosome locus (Q35879331) (← links)
- Molecular characterization of the marker chromosome associated with cat eye syndrome (Q35889314) (← links)
- A large deletion encompassing the entire alpha-like globin gene cluster in a family of northern European extraction (Q36077209) (← links)
- A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library (Q36414869) (← links)
- Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to human chromosome 12q. (Q36424470) (← links)