| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/0888-7543(92)90370-8 |
| P698 | PubMed publication ID | 1339384 |
| P50 | author | Jonathan L Haines | Q73570557 |
| James F. Gusella | Q1602688 | ||
| P2093 | author name string | D. J. Kwiatkowski | |
| L. Ozelius | |||
| J. Haines | |||
| E. P. Henske | |||
| K. Weimer | |||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | repetitive DNA | Q424473 |
| human chromosome 9 | Q840604 | ||
| P304 | page(s) | 229-240 | |
| P577 | publication date | 1992-02-01 | |
| P1433 | published in | Genomics | Q5533503 |
| P1476 | title | Construction of a GT polymorphism map of human 9q | |
| P478 | volume | 12 |
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| Q72372689 | A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3 |
| Q30741023 | A genetic linkage map of human chromosome 9q |
| Q34044602 | A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. |
| Q41614667 | A radiation-reduced hybrid cell line containing 5 Mb/17 cM of human DNA from 9q34 |
| Q38299272 | A simple method for rapid isolation of microsatellites from yeast artificial chromosomes |
| Q36721045 | Abundance, polymorphism and genetic mapping of microsatellites in rice |
| Q33960599 | Allele frequencies at microsatellite loci: the stepwise mutation model revisited |
| Q35881966 | Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions |
| Q35195141 | An index marker map of chromosome 9 provides strong evidence for positive interference |
| Q80100934 | Analysis of differentially expressed genes in neuroendocrine carcinomas of the lung |
| Q53205346 | Assessment of genetic polymorphisms in DNA from formalin fixed neurological tissues. |
| Q44002208 | Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder? |
| Q35273392 | Biogeographic range expansion into South America by Coccidioides immitis mirrors New World patterns of human migration |
| Q71612288 | Chromosome 10 allelic loss in malignant melanoma |
| Q35796194 | Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas |
| Q72698569 | DNA typing of grapevines: a universal methodology and database for describing cultivars and evaluating genetic relatedness |
| Q35061023 | Dinucleotide repeat polymorphism at the D9S112 locus (9q31-34) |
| Q35061059 | Dinucleotide repeat polymorphism at the D9S115 locus (9q31-34) |
| Q35061096 | Dinucleotide repeat polymorphism at the D9S116 locus (9q31-34). |
| Q35061135 | Dinucleotide repeat polymorphism at the D9S117 locus (9q31-34). |
| Q35061167 | Dinucleotide repeat polymorphism at the D9S118 locus (9q31-34) |
| Q35061208 | Dinucleotide repeat polymorphism at the D9S119 locus (9q22-34). |
| Q35061239 | Dinucleotide repeat polymorphism at the D9S120 locus (9q31-34) |
| Q35061255 | Dinucleotide repeat polymorphism at the D9S121 locus (9q31-34) |
| Q35061295 | Dinucleotide repeat polymorphism at the D9S123 locus (9q31-34) |
| Q24655175 | Equilibrium distributions of microsatellite repeat length resulting from a balance between slippage events and point mutations |
| Q30445566 | Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere |
| Q35194779 | Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19. |
| Q34740224 | Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium |
| Q35239250 | Fine mapping of the nail-patella syndrome locus at 9q34 |
| Q34638183 | Genetic alterations in colorectal cancer. |
| Q34722031 | Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population |
| Q34385650 | Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3. |
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| Q33968396 | Genetic distances and reconstruction of phylogenetic trees from microsatellite DNA. |
| Q71578944 | Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations |
| Q21563514 | Genomic variability within an organism exposes its cell lineage tree |
| Q67982145 | Identification and localization of microsatellite markers covering human chromosome 18 |
| Q22009978 | Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1 |
| Q33595104 | Identification of markers flanking the tuberous sclerosis locus on chromosome 9 (TSC1). |
| Q33595312 | Linkage analysis of infantile pyloric stenosis and markers from chromosome 9q11-q33: no evidence for a major gene in this candidate region |
| Q35643780 | Linkage analysis of the nail-patella syndrome |
| Q35194459 | Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes |
| Q41452308 | Linkage disequilibrium patterns vary with chromosomal location: a case study from the von Willebrand factor region. |
| Q33594756 | Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, 11q, and 12q. The Tuberous Sclerosis Collaborative Group |
| Q64461903 | Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14q |
| Q28208062 | Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease |
| Q35644386 | Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study Group. |
| Q33596285 | Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneity |
| Q28257920 | Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33 |
| Q35643486 | Localization of an ataxia-telangiectasia gene to an approximately 500-kb interval on chromosome 11q23.1: linkage analysis of 176 families by an international consortium |
| Q52224929 | Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis. |
| Q38559869 | Low mutation rates of microsatellite loci in Drosophila melanogaster |
| Q53178836 | Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3 |
| Q52073873 | Markers and methods for reconstructing modern human history. |
| Q42632071 | Methylation of CpG island transcription factor binding sites is unnecessary for aberrant silencing of the human MGMT gene |
| Q41489842 | Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11p and 17p in medulloblastomas |
| Q72048133 | Microsatellite evolution — evidence for directionality and variation in rate between species |
| Q36422746 | Microsatellite instability and loss of heterozygosity in mammary carcinoma and its probable precursors |
| Q42026610 | Microsatellite instability in human prostate cancer |
| Q72787989 | Microsatellite markers and the analysis of genetic disease |
| Q86651746 | Microsatellite repeats in grapevine reveal DNA polymorphisms when analysed as sequence-tagged sites (STSs) |
| Q36780262 | Microsatellite variation in a social insect |
| Q48068910 | Microsatellite variation in grey seals (Halichoerus grypus) shows evidence of genetic differentiation between two British breeding colonies |
| Q47795731 | Molecular markers for reinforcement of histological subclassification of neuroendocrine lung tumors |
| Q70732495 | Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry |
| Q52016712 | Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelic |
| Q37091218 | Mutation rate varies among alleles at a microsatellite locus: phylogenetic evidence |
| Q35159058 | Mutational processes of simple-sequence repeat loci in human populations. |
| Q41500422 | New alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines |
| Q33735682 | Non-DYT1 dystonia in a large Italian family |
| Q43146454 | Perils of gene mapping with microsatellite markers |
| Q70597601 | Phylogenetic distribution and genetic mapping of a (GGC)n microsatellite from rice (Oryza sativa L.). |
| Q45094448 | Polymorphism and phylogeny of dinucleotide repeats in human T-cell receptor Vb6 genes |
| Q34389378 | Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31 |
| Q48830604 | Prenatal diagnosis of Fukuyama type congenital muscular dystrophy by polymorphism analysis |
| Q35889527 | Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium. |
| Q35968680 | Relative mutation rates at di-, tri-, and tetranucleotide microsatellite loci |
| Q30443033 | Report of a critical recombination further narrowing the TSC1 region |
| Q67482087 | Somatic mutations at CA-repeat loci |
| Q73247971 | Strong association between microsatellites and an HLA-B, DR haplotype (B18-DR3): implication for microsatellite evolution |
| Q35643518 | Sublocalization of an ataxia-telangiectasia gene distal to D11S384 by ancestral haplotyping in Costa Rican families |
| Q72220263 | Support for founder effect for two lipoprotein lipase (LPL) gene mutations in French Canadians by analysis of GT microsatellites flanking the LPL gene |
| Q35889685 | The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews |
| Q41659448 | The canine genome |
| Q35782131 | Tuberous sclerosis-associated renal cell carcinoma. Clinical, pathological, and genetic features |
| Q35889650 | Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation |
| Q36794239 | Unusually high frequency of (CT)n and (GT)n microsatellite loci in a yellowjacket wasp, Vespula rufa (L.) (Hymenoptera: Vespidae). |
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