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Trisomy

  • The Mutational Landscape of Myeloid Leukaemia in Down Syndrome

    The Mutational Landscape of Myeloid Leukaemia in Down Syndrome

  • Adult Acute Myeloid Leukemia with Trisomy 11 As the Sole Abnormality

    Adult Acute Myeloid Leukemia with Trisomy 11 As the Sole Abnormality

  • ABC of Clinical Genetics CHROMOSOMAL DISORDERS II

    ABC of Clinical Genetics CHROMOSOMAL DISORDERS II

  • Dr. Fern Tsien, Dept. of Genetics, LSUHSC, NO, LA Down Syndrome

    Dr. Fern Tsien, Dept. of Genetics, LSUHSC, NO, LA Down Syndrome

  • Cytogenetics, Chromosomal Genetics

    Cytogenetics, Chromosomal Genetics

  • Paternally Inherited Trisomy at D21S11 and Mutation at DXS10135 Microsatellite Marker in a Case of Fetus Paternity Establishment

    Paternally Inherited Trisomy at D21S11 and Mutation at DXS10135 Microsatellite Marker in a Case of Fetus Paternity Establishment

  • ©Ferrata Storti Foundation

    ©Ferrata Storti Foundation

  • NIPT Fact Sheet

    NIPT Fact Sheet

  • Trisomy 8 Mosaicism

    Trisomy 8 Mosaicism

  • Chromosome Mutations Definitions a Mutation Is Any Change in the DNA

    Chromosome Mutations Definitions a Mutation Is Any Change in the DNA

  • Chromosomal Disorders

    Chromosomal Disorders

  • NIPT Fact Sheet

    NIPT Fact Sheet

  • Trisomy 13 (Patau Syndrome)

    Trisomy 13 (Patau Syndrome)

  • Trisomy 14 Mosaicism FTNW

    Trisomy 14 Mosaicism FTNW

  • The Physical and Genetic Components of Intersex

    The Physical and Genetic Components of Intersex

  • A Case of Partial 5Q Trisomy Associated with Partial 7Q Monosomy

    A Case of Partial 5Q Trisomy Associated with Partial 7Q Monosomy

  • Functional Analysis of Mutations of Murine Chromosome 17 with the Use of Tertiary Trisomy

    Functional Analysis of Mutations of Murine Chromosome 17 with the Use of Tertiary Trisomy

  • Trisomy 18 – Edwards Syndrome

    Trisomy 18 – Edwards Syndrome

Top View
  • The 'D' (13-15) Trisomy Syndrome: an Analysis of 7 Examples G
  • Syndrome Review 1: Autosomal Trisomies and Sex Chromosome
  • Bleeding Disorders in Congenital Syndromes Susmita N
  • SALSA® MLPA® Probemix P245-B1 Microdeletion Syndromes-1A to Be Used with the MLPA General Protocol
  • Variants and Health
  • A Guide for Parents
  • Prenatal Screening for Fetal Aneuploidy AHS – G2055
  • 45,X/46,XY/47,XY,+21 Mosaicism in a Hypogonadal Phenotypic Male
  • A Mother with Variant Turner Syndrome and Two Daughters with Trisomy X: a Case Report
  • HHS Public Access Author Manuscript
  • Sex Chromosome Problems Discovered Through Prenatal Testing
  • Double Aneuploidy: a Case of Trisomy 21 with XYY
  • New Humandouble Trisomy Or Tetrasomy
  • NIH Research Plan on Fragile X Syndrome and Associated Disorders
  • Diagnostic Testing and Screening
  • Multiple Aneuploidies
  • Sex Chromosome Abnormalities
  • Trisomy 13 — Patau Syndrome


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