Abstracts: Classification of familial adenomatous polyposis: a diagnostic nightmare. A common genetic mechanism determines plasma apolipoprotein B levels and dense LDL subfraction distribution in familial combined hyperlipidemia
Abstracts: The hemochromatosis 845 G-->A and 187 C-->G mutations: prevalence in non-Caucasian populations. Mitochondrial and nuclear genetic relationships among Pacific Island and Asian populations
Abstracts: Girl talk: 'Jane Eyre' and the romance of women's narration. Jane Eyre and the secrets of furious lovemaking
Abstracts: Pharmacogenetics of cancer therapy: getting personal. Epigenetic regulation of human gamma-glutamyl hydrolase activity in acute lymphoblastic leukemia cells
Abstracts: The spreading of X-inactivation into autosomal material of an X;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA
Abstracts: Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA. Autosomal dominant cerebellar ataxia type III: Linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3
Abstracts: Maternal mosaicism for a second mutational event in a type I spinal muscular atrophy family. Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling
Abstracts: Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap in chromosome 22q11
Abstracts: Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family
Abstracts: A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3
Abstracts: PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Linkage and association between inflammatory bowel disease and a locus on chromosome 12
Abstracts: X-linked chronic granulomatous disease: mutations in the CYBB (ital) gene encoding the gp91-phox(ital) component of respiratory-burst oxidase
Abstracts: The SEC attacks abuses in the use of Form S-8 registration statement. Re-visiting the question: must a broker-dealer securities firm use another broker-dealer securities firm in selling its own restricted securities under Rule 144
Abstracts: Marker selection for the transmission/disequilibrium test, in recently admixed populations. Linkage disequilibrium and gene mapping: an empirical least-squares approach
Abstracts: Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11
Abstracts: Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22
Abstracts: Direct evidence for suppression of recombination within two pericentric inversions in humans: a new sperm-FISH technique
Abstracts: DNA variation in a 5-Mb region of the X chromosome and estimates of sex-specific/type-specific mutation rates
Abstracts: Power of association and linkage tests when the disease alleles are unobserved. Mapping genes that underlie ethnic differences in disease risk: methods for detecting linkage in admixed populations, by conditioning on parental admixture
Abstracts: Multipoint oligogenic analysis of age-at-onset data with applications to Alzheimer disease pedigrees. Inflation of sibling recurrence-risk ratio, due to ascertainment bias and/or overreporting
Abstracts: A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. PedCheck: a program for identification of genotype incompatibilities in linkage analysis
Abstracts: Cytosine methylation and the unequal developmental potentials of the oocyte and sperm genomes. The molecular basis of vascular disorders
Abstracts: Male infertility and the genetics of spermatogenesis. Genetic mapping of ossification of the posterior longitudinal ligament of the spine
Abstracts: Insights from model systems: the yeast connection to Friedrich ataxia. Insights from model systems: genetic causes of female infertility: targeted mutagenesis in mice
Abstracts: Classification of familial adenomatous polyposis: a diagnostic nightmare. part 2 Genotype-phenotype correlations in attenuated adenomatous polyposis coli
Abstracts: Inherited colorectal polyposis and cancer risk of the APC I1307K (ital) polymorphism. Genotype-phenotype correlations in attenuated adenomatous polyposis coli
Abstracts: Modification of BRCA1 (ital)-associated breast cancer risk by the polymorphic androgen-receptor CAG repeat. Hyperphenylalaninemia with high levels of 7-biopterin is associated with mutations in the PCBD (ital) gene encoding the bifunctional protein pterin -4a carbinolamine dehydratase and transcriptional coactivator (DCoH)
Abstracts: Structure of the GM2A (ital) gene: identification of an exon 2 nonsense mutation and a naturally occurring transcript with an in-frame deletion of exon 2
Abstracts: X-linked chronic granulomatous disease: mutations in the CYBB (ital) gene encoding the gp91-phox(ital) component of respiratory-burst oxidase. part 2
Abstracts: Novel molecular variants of the Na-K-2C cotransporter gene are responsible for antenatal Bartter syndrome. Genotype-phenotype relationships in ataxia-telangiectasia and variants
Abstracts: Analysis of alkaptonuria (AKU) mutations and polymorphisms reveals that the CCC sequence motif is a mutational hot spot in the homogentisate 1,2 dioxygenase gene (HGO) (ital)
Abstracts: A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations
Abstracts: Juvenile hemochromatosis locus maps to chromosome 1q. Identification of microdeletions spanning the Diamond-Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity
Abstracts: Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36. Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43
Abstracts: A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset
Abstracts: Making mindful managers: evaluating methods for teaching problem solving skills for tourism management. Interpretation and sustainable tourism: functions, examples and principles
Abstracts: Taxation with an attitude: can we rationalize the distinction between "earned" and "unearned" income? Tax breaks for higher education: tax policy or tax pandering?
Abstracts: Hyperparathyroidism-jaw tumor syndrome: the HRPT2 (ital) locus is within a 0.7-cM region on chromosome 1q. Genetic mapping of ossification of the posterior longitudinal ligament of the spine
Abstracts: Haplotype mapping of a major quantitative-trait locus for fetal hemoglobin production, on chromosome 6q23. Osteoarthritis-susceptibility locus on chromosome 11q, detected by linkage
Abstracts: An alternative route for multistep tumorigenesis in a novel case of hereditary renal cell cancer and a t(2;3)(q35;q21) chromosome translocation
Abstracts: Brachydactyly type B: linkage to chromosome 9q22 and evidence for genetic heterogeneity. Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3
Abstracts: Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome
Abstracts: Identification of cryptic rearrangements in patients with 18q- deletion syndrome. Evidence for a novel osteosarcoma tumor-suppressor gene in the chromosome 18 region genetically linked with Paget disease of bone
Abstracts: Dating the origin of the CCR5-delta32 (ital) AIDS-resistance allele by the coalescence of haplotypes. Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population
Abstracts: Splice-site mutations: a novel genetic mechanism of Crigler-Najjar syndrome type 1. Missense mutations in disease genes: a Bayesian approach to evaluate causality
Abstracts: Useful Web sites for the real estate professional: historical data. Useful sites on the Internet
Abstracts: Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population
Abstracts: Mitochrondrial dysfunction in idiopathic Parkinson disease. Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q
Abstracts: Are we ready to try to cure alkaptonuria? A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32
Abstracts: Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlation
Abstracts: OA1 (ital) mutations and deletions in X-linked ocular albinism. Autosomal dominant nanophthalmos (NNO1 (ital)) with high hyperopia and angle-closure glaucoma maps to chromosome 11
Abstracts: Marshall syndrome associated with a splicing defect at the COL11A1 (ital) locus. A clinical variant of neurofibromatosis type 1: familial spinal neurofibromatosis with a frameshift mutation in the NF1 (ital) gene
Abstracts: Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
Abstracts: A clinical variant of neurofibromatosis type 1: familial spinal neurofibromatosis with a frameshift mutation in the NF1 (ital) gene
Abstracts: A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset. part 2
Abstracts: Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28. Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosis
Abstracts: Mapping of primary congenital lymphedema to the 5q35.3 region. Evidence for genetic heterogeneity in X-linked congenital stationary night blindness
Abstracts: Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34
Abstracts: Quantitative analysis of survival motor neuron copies: identification of subtle SMN1 (ital) mutations in patients with spinal muscular atrophy, genotype-phenotype correlation, and implications for genetic counseling
Abstracts: Deletions within COL7A1 exons distant from consensus splice sites alter splicing and produce shortened polypeptides in dominant dystrophic epidermolysis bullosa
Abstracts: Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15. A Huntington disease-like neurodegenerative disorder maps to chromosome 20p
Abstracts: Using neural networks as an aid in the determination of disease status: comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-girdle muscular dystrophy
Abstracts: Genetic association mapping based on discordant sib pairs: the discordant-alleles test. A comparative study of sibship tests of linkage and/or association
Abstracts: Further evidence for the increased power of LOD scores compared with nonparametric methods. A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting
Abstracts: Molecular prophets of death in the fly. The promoters of the survival motor neuron gene (SMN)(ital) and its copy (SMNc)(ital) share common regulatory elements
Abstracts: An artful child: how music, drama and art add richness to kids' lives - and build brainpower. Nurturing the power of make-believe
Abstracts: Making lessons from lemonade. Thriving in tough times. How to help your kids live as well as (or better than) you: what you need to know - and teach your children - to give them a financially secure future
Abstracts: The right size type depends upon your readership, the typeface you are using, your page layout, even how you print your paper...
Abstracts: Small paper: big changes. Our World Cup winners. Back to basics
Abstracts: Mechanisms of cell death in the inherited retinal degenerations. Molecular prophets of death in the fly
Abstracts: A gene for lymphedema-distichiasis maps to 16q24.3. A new twist: some patients with Saethre-Chotzen syndrome have a microdeletion syndrome
Abstracts: Comprehensive mutation analysis of TSC1 (ital) and TSC2 (ital)--and phenotypic correlations in 150 families with tuberous sclerosis
Abstracts: Genome search in celiac disease. X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats
Abstracts: Flexing DNA: HMG-box proteins and their partners. Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populations
Abstracts: Rh(sub.mod) syndrome: a family study of the translation-initiator mutation in the Rh50 glycoprotein gene. Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P3401B1
Abstracts: Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population
Abstracts: Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlation. part 2
Abstracts: Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling. Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set
Abstracts: Will she ever learn to use the potty? How to overcome the 5 biggest toilet-training challenges. 3 easy stages: a guide to potty training
Abstracts: 5 ways to get dads to pull their weight. Away we go. New parents' survival guide
Abstracts: Financial growing pains. The value of play money. The going rate
Abstracts: Localization of familial benign hypercalcemia, Oklahoma variant (FBH (sub.Ok)), to chromosome 19q13. Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28
Abstracts: Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q
Abstracts: ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer
Abstracts: Comparison of the power and accuracy of biallelic and microsatellite markers in population-based gene-mapping methods
Abstracts: Talking taxes: Tim Morris, of Revisuisse Price Waterhouse, answers expats' questions. Talking taxes: Lars-Olaf Timmermann, of Arthur Andersen, answers expats' questions
Abstracts: Domestic appliances and consumer electronics in France. Domestic appliances and consumer electronics in Belgium
Abstracts: Domestic appliances and consumer electronics in the Netherlands. Domestic appliances and consumer electronics in France
Abstracts: Phase behaviour of model stratum corneum lipid mixtures: an infrared spectroscopy investigation. 2H NMR studies of dipalmitoylphosphatidylcholine and dipalmitoylphosphatidylcholine--cholesterol bilayers at high pressure
Abstracts: Characterization of macroscopic disorder in a porous glass with NMR microimaging and scanning electron microscopy
Abstracts: Irradiance and temperature dependence of photoinduced orientation in two azobenzene-based polymers. Evidence for room temperature mesomorphism in a mixed-valent diruthenium(II, III) quintapalmitoleate polymer
Abstracts: Charge-transfer phenomena in holographic recording material: dichromated poly(acrylic acid). Synthesis and properties of a sterically encumbered poly(thienylene vinylene): poly (E-1,2-(4,4'-dihexyl-2,2'-dithienyl)ethylene)
Abstracts: Electrochemical study of the pore structure of sandstone and similar media. Characterization of macroscopic disorder in a porous glass with NMR microimaging and scanning electron microscopy
Abstracts: A solid state 31P NMR study of the synthesis of phosphorus sulfides from PCl3 and H2S in microporous materials
Abstracts: Molecular self-assembly of rigid-rod alkynyl chromophores on inorganic oxide surfaces. Vibrational spectra and structure of tris(8-hydroxyquinoline)aluminum(III)
Abstracts: Mammoth hunter. Mercury rising. Monkey man
Abstracts: OECD bribery convention. Convention on combating bribery of foreign public officials. What the OECD Convention means for American business
Abstracts: The Bayesian approach to an internally consistent thermodynamic database: theory, database, and generation of phase diagrams
Abstracts: The value relevance of intangibles: the case of software capitalization. Information asymmetry, R&D, and insider gains
Abstracts: Revalued financial, tangible, and intangible assets: associations with share prices and non-market-based value estimates
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