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Uniparental disomy

  • Robertsonian Translocations FTNW

    Robertsonian Translocations FTNW

  • Sema4 Noninvasive Prenatal Select

    Sema4 Noninvasive Prenatal Select

  • Fragile X Syndrome

    Fragile X Syndrome

  • Inheriting Genetic Conditions

    Inheriting Genetic Conditions

  • Mosaic Genome-Wide Maternal Isodiploidy: an Extreme Form Of

    Mosaic Genome-Wide Maternal Isodiploidy: an Extreme Form Of

  • Risk Estimation of Uniparental Disomy of Chromosome 14 Or 15 in a Fetus with a Parent Carrying a Non-Homologous Robertsonian Translocation

    Risk Estimation of Uniparental Disomy of Chromosome 14 Or 15 in a Fetus with a Parent Carrying a Non-Homologous Robertsonian Translocation

  • PRENATAL DIAGNOSIS of PATERNAL UNIPARENTAL ISODISOMY of CHROMOSOME 14 (Patiupd14) with CHROMOSOMAL MICRO-ARRAY in a FETUS with MULTIPLE CONGENITAL ABNORMALITIES

    PRENATAL DIAGNOSIS of PATERNAL UNIPARENTAL ISODISOMY of CHROMOSOME 14 (Patiupd14) with CHROMOSOMAL MICRO-ARRAY in a FETUS with MULTIPLE CONGENITAL ABNORMALITIES

  • Copy-Neutral Loss of Heterozygosity and Chromosome Gains and Losses

    Copy-Neutral Loss of Heterozygosity and Chromosome Gains and Losses

  • Maternal Uniparental Disomy of Chromosome 20 (UPD(20)Mat) As Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases

    Maternal Uniparental Disomy of Chromosome 20 (UPD(20)Mat) As Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases

  • Chromosomal Disorders

    Chromosomal Disorders

  • Frequent Occurrence of Uniparental Disomy in Colorectal Cancer

    Frequent Occurrence of Uniparental Disomy in Colorectal Cancer

  • Uniparental Disomy (UPD)

    Uniparental Disomy (UPD)

  • A Search for Uniparental Disomy in Carriers of Supernumerary Marker

    A Search for Uniparental Disomy in Carriers of Supernumerary Marker

  • Identification of Paternal Uniparental Disomy on Chromosome 22 and A

    Identification of Paternal Uniparental Disomy on Chromosome 22 and A

  • Diagnostic Testing for Uniparental Disomy: a Points to Consider Statement from the American College of Medical Genetics and Genomics (ACMG)

    Diagnostic Testing for Uniparental Disomy: a Points to Consider Statement from the American College of Medical Genetics and Genomics (ACMG)

  • A Placental Diploid Cell Line Is Not Essential for Ongoing Trisomy 13 Or

    A Placental Diploid Cell Line Is Not Essential for Ongoing Trisomy 13 Or

  • And Uniparental Disomy (UPD): Coincidence Or Consequence? D Kotzot

    And Uniparental Disomy (UPD): Coincidence Or Consequence? D Kotzot

  • Syndrome of the Month

    Syndrome of the Month

Top View
  • Sex Linked Diseases
  • General Information About Positive NIPT Results
  • Chromosomal Abnormalities and Mental Illness
  • Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population
  • Patterns and Frequencies of Acquired and Constitutional Uniparental Isodisomies in Pediatric and Adult B-Cell Precursor Acute Lymphoblastic Leukemia
  • Uniparental Disomy
  • Uniparental Disomy (UPD) Tech Review.Indd
  • Molecular Allelokaryotyping of Relapsed Pediatric Acute Lymphoblastic Leukemia
  • Low Incidence of UPD in Spontaneous Abortions Beyond the 5Th Gestational Week
  • Paternal Uniparental Disomy of Chromosome 14 and Unique Exchange of Chromosome 7 in Cases of Spontaneous Abortion
  • Chromosomal Mosaicism and Uniparental Disomy in Prenatal Diagnosis: Clinical Implications for Genetic Counseling
  • Methylation Analysis (Of Chromosomes 14 and 15)
  • Applications of Genome Editing Technology in Research on Chromosome Aneuploidy Disorders
  • Cytogenetics Into Cytogenomics: SNP Arrays Expand the Screening Capabilities of Genetics Laboratories Contributed by Laura K
  • Non-Mendelian Inheritance
  • Letter Advance Publication DOI: 10.5582/Irdr.2016.01043
  • Mosaicism for Trisomy 21: a Review
  • Clinical Relevance of Screening for Rare Autosomal Aneuploidies: a Case of Maternal Uniparental Disomy J


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