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    Human Reproductive and Prenatal Genetics

    Human Reproductive and Prenatal Genetics

    Forfatter: info mangler
    Bog
    • Format
    • Bog, paperback
    • Engelsk

    Beskrivelse

    Human Reproductive and Prenatal Genetics presents the latest material from a detailed molecular, cellular and translational perspective. Considering its timeliness and potential international impact, this all-inclusive and authoritative work is ideal for researchers, students, and clinicians worldwide. Currently, there are no comprehensive books covering the field of human reproductive and prenatal genetics. As such, this book aims to be among the largest and most useful references available. Named a Highly Commended book in the Basic and Clinical Sciences by the British Medical Association.

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    Detaljer
    • SprogEngelsk
    • Sidetal709
    • Udgivelsesdato29-08-2018
    • ISBN139780128135709
    • Forlag Academic Press Inc
    • FormatPaperback
    Størrelse og vægt
  • Vægt1680 g
    • coffee cup img
    10 cm
    book img
    19,1 cm
    23,5 cm

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    Transplantation Pregnancy Infertility Fertility Aging Gene expression. Genetics Genomics Menopause Molecular genetics Reproduction Germ cells Hypogonadism Transcription factors Differentiation Uterus Endometriosis Down syndrome Pregnancy Complications Prenatal diagnosis Embryos Genetic counseling Polycystic ovary syndrome Genomic imprinting Embryonic stem cells Chromatin Maternal age Placenta Spermatogenesis Embryo Implantation Fertilization Histones Hypospadias Mitochondrial Diseases Mitosis Recurrence DNA Methylation Talen Meiosis Endocrine disrupting chemicals Genetic Testing Induced Pluripotent Stem Cells Aneuploidy Epigenetics Oocytes Oogenesis hr Transcriptome MicroRNA Human sperm Transgenerational inheritance Chromosome Imprinting Trophoblast Congenital Adrenal Hyperplasia In vitro-Fertilisation Ovarian function CRISPR/CAS9 Genome sequencing Telomeres Whole genome sequencing Gametes Array-CGH Phenome Germline Germ Cell Noncoding RNA SNPs Primordial germ cells Primary ovarian insufficiency Biomarkers Fetal programming Epigenetic Endometrial receptivity In vitro spermatogenesis Fetal aneuploidy Monogenic disease Male Infertility GWAS Cryptorchidism Intergenerational Transmission DNA recombination In-Vitro Fertilization Gene Polymorphism Oocyte maturation Adenomyosis Exome sequencing SiRNA Recurrent pregnancy loss Transcriptomics Histone modification Gonads Fetal anomalies Prematurity Incidental findings Chromosomal aberration Noncoding RNAs Phthalate Assisted reproduction Biomarker CMA MiRNAs Oocyte Chromosomal microarray Genetic predisposition Preimplantation genetic testing Azoospermia Premature ovarian failure Bardet-Biedl syndrome Monogenic diseases Klinefelter Exposome PGS NHEJ Analytical validity Aneuploid Bicornuate Cell-free fetal DNA Blood heavy metals CNVs Chromosome instability Cell-free DNA testing technologies Decidualization Developmental competence Candidate gene studies DSBs DES Exposure EPAB Discordant results Fallopian tube anomalies Family-centered management approach clinical utility Fetal loss Embryo health clinical validity Epipolymorphism Fetal fraction measurement CPEB Cytoplasmic polyadenylation Fetal WES CYP21A2 gene Genital Tubercle Hand-foot-genital syndrome Didelphys Hypothesis of unfavorable genomes Early gonad development Endometrial fluid Establishment of DNA methylation Invasive prenatal diagnosis MtDNA diseases Maskin Meiotic kinetochore Gene panels mRNA degradation mRNA translation regulation Mayer-Rokitanski-Kuster-Hauser syndrome Microdeletions noninvasive Noninvasive prenatal diagnosis Mitochondrial inheritance No results Plasma DNA Gene-environmental interaction ovarian development OxidativePlease check if the suggested by the editor are appropriate. If not Rare chromosome imbalances RINGO/spy SNP microarray RNA-binding protein Male sex differentiation Translation regulation Ultrasound anomalies Vaginal Agenesis Microarray-based analysis Y microdeletion Zygotic genome activation Prenatal aneuploidy screening McKusick-Kaufman syndrome Mosacism Pathogenic Variants Noninvasive prenatal testing Products of conception Transcriptome of chorionic villi Placental epigenome please provide no more than 6-8 .--> Posttranscriptional ZFNs Variants of uncertain significance Unicornuate Wolffian duct remnant Testicular Descent Window of implantation

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