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Chromosome 18

  • 18P Deletions FTNW

    18P Deletions FTNW

  • Chromosome 18

    Chromosome 18

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  • Epigenetic Abnormalities Associated with a Chromosome 18(Q21-Q22) Inversion and a Gilles De La Tourette Syndrome Phenotype

    Epigenetic Abnormalities Associated with a Chromosome 18(Q21-Q22) Inversion and a Gilles De La Tourette Syndrome Phenotype

  • Human Artificial Chromosomes Generated by Modification of a Yeast Artificial Chromosome Containing Both Human Alpha Satellite and Single-Copy DNA Sequences

    Human Artificial Chromosomes Generated by Modification of a Yeast Artificial Chromosome Containing Both Human Alpha Satellite and Single-Copy DNA Sequences

  • White Matter Changes Associated with Deletions of the Long Arm of ?Chromosome 18 (18Q؊ Syndrome): a Dysmyelinating Disorder

    White Matter Changes Associated with Deletions of the Long Arm of ?Chromosome 18 (18Q؊ Syndrome): a Dysmyelinating Disorder

  • Chromosome (Mis)Segregation Is Biased by Kinetochore Size

    Chromosome (Mis)Segregation Is Biased by Kinetochore Size

  • Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings

    Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings

  • Psychiatric Syndromes in Individuals with Chromosome 18 Abnormalities

    Psychiatric Syndromes in Individuals with Chromosome 18 Abnormalities

  • Genetic Linkage and Bipolar Affective Disorder: Progress and Pitfalls M Baron

    Genetic Linkage and Bipolar Affective Disorder: Progress and Pitfalls M Baron

  • Receptor Signaling Through Osteoclast-Associated Monocyte

    Receptor Signaling Through Osteoclast-Associated Monocyte

  • A Simple Method to Allow for Guanine-Cytosine Amplification Error

    A Simple Method to Allow for Guanine-Cytosine Amplification Error

  • GENE LIST ANTI-CORRELATED Systematic Common Description

    GENE LIST ANTI-CORRELATED Systematic Common Description

  • Trisomy 18 – Edwards Syndrome

    Trisomy 18 – Edwards Syndrome

  • A Comprehensive Genetic Map of Murine Chromosome 11 Reveals Extensive Linkage Conservation Between Mouse and Human

    A Comprehensive Genetic Map of Murine Chromosome 11 Reveals Extensive Linkage Conservation Between Mouse and Human

  • 18 Chromosome Chapter

    18 Chromosome Chapter

  • Extreme Reduction of Chromosome-Specific Α-Satellite Array Is Unusually Common in Human Chromosome 21

    Extreme Reduction of Chromosome-Specific Α-Satellite Array Is Unusually Common in Human Chromosome 21

  • Ring 18 FTNW

    Ring 18 FTNW

Top View
  • Abnormalities of Chromosome 18 in a Girl with Mental Retardation and Autistic Disorder M
  • Basic Principles of Human Genetics: a Primer for Oral Medicine Harold C
  • The Trisomy 18 Syndrome Anna Cereda1 and John C Carey2*
  • Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
  • Centromere Repeats: Hidden Gems of the Genome
  • Human Chromosome 18 and Acrocentrics: a Dangerous Liaison
  • Three Cep18 Fish Signals in Amniocytes and a Clinically Normal Fetus
  • Proximal 18Q Deletion Syndrome
  • View Our Flipbook
  • Adults with Chromosome 18 Abnormalities
  • Impaired CENP-E Function Renders Large Chromosomes More Vulnerable to Congression Failure
  • Uniparental Propagation of Mitochondrial DNA in Mouse-Human Cell Hybrids
  • 18Q Deletions from 18Q11.2 to 18Q21.2
  • 18Q Deletions: from 18Q21 and Beyond
  • Trisomy 18 Syndrome with an Unusual Karyotype
  • Help Me Understand Genetics
  • 10P Deletions FTNW
  • A Gene Dosage Map of Chromosome 18: a Map with Clinical Utility Jannine D


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