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1. Full Text A practical guide to fetal echocardiography
: normal and abnormal hearts
by Abuhamad, Alfred, author and Chaoui, Rabih, author
2016, Third edition., ISBN 1451176058, 944
Heart Defects, Congenital | Ultrasonography, Prenatal | ultrasonography | methods | Fetal Heart | Fetal heart | Ultrasonic imaging
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2. Antenatal and neonatal screening
by Leck, Ian and Wald, Nicholas J
2000, 2nd ed., ISBN 0192628267, xxii, 591
Pregnancy | Prenatal diagnosis | Newborn infants | Diagnosis | Complications | Diseases | Epidemiology | Public Health | Problems areas | Antenatal screening | Neontal screening | Technical procedures | Efficacy | Abnormality detection | Safety | Research needs
Book
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3. Full Text 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy The Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC)
by Elliott, Perry M and Anastasakis, Aris and Borger, Michael A and Borggrefe, Martin and Cecchi, Franco and Charron, Philippe and Hagege, Albert Alain and Lafont, Antoine and Limongelli, Giuseppe and Mahrholdt, Heiko and McKenna, William J and Mogensen, Jens and Nihoyannopoulos, Petros and Nistri, Stefano and Pieper, Petronella G and Pieske, Burkert and Rapezzi, Claudio and Rutten, Frans H and Tillmanns, Christoph and Heymans, Stephane and Watkins, Hugh and Authors/Task Force members
European heart journal, ISSN 0195-668X, 10/2014, Volume 35, Issue 39, pp. 2733 - 2779
Heart failure | Hypertension | Valve disease | Arrhythmia | Left ventricular outflow tract obstruction | Sudden cardiac death | Athletes | Guidline | Pregnancy | Cardiac imaging | Genetics | Diagnosis | Symptoms | Implantable cardioverter defibrillators | Guideline | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Physical Examination - methods | Humans | Death, Sudden, Cardiac - prevention & control | Angina Pectoris - etiology | Genetic Testing - methods | Ventricular Outflow Obstruction - etiology | Sports Medicine | Adult | Female | Heart Valve Diseases - diagnosis | Cardiac Imaging Techniques - methods | Pregnancy Complications, Cardiovascular - diagnosis | Cardiomyopathy, Hypertrophic - etiology | Cardiomyopathy, Hypertrophic - therapy | Child | Heart Failure - etiology | Electrocardiography - methods | Pregnancy Complications, Cardiovascular - therapy | Diagnosis, Differential | Prenatal Care - methods | Risk Factors | Genetic Counseling - methods | Medical History Taking - methods | Arrhythmias, Cardiac - etiology | Cardiac Pacing, Artificial - methods | Cardiomyopathy, Hypertrophic - diagnosis | Clinical Laboratory Techniques - methods | Ablation Techniques - methods | Delivery of Health Care | Pedigree | Syncope - etiology | Heart Valve Diseases - therapy | Preconception Care - methods | Thoracic Surgical Procedures - methods | Index Medicus | Medicin och hälsovetenskap
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4. Reproductive health and human rights
: integrating medicine, ethics, and law
by Cook, Rebecca J and Dickens, Bernard M., 1937 and Fathalla, Mahmoud F
2003, Issues in biomedical ethics, ISBN 9780199241323, xxvii, 554
Moral and ethical aspects | Human reproduction | Medical ethics | Human reproductive technology | Moral Philosophy | Bioethics and Medical Ethics | Social and Political Philosophy | Women | Ethics | Reproductive Health | Health Care Provision | Human Rights | Medical Law | Legal Protection
Book
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5. Reducing the odds
: preventing perinatal transmission of HIV in the United States
by Almario, Donna A and McCormick, Marie C and Stoto, Michael A and Institute of Medicine (U.S.). Committee on Perinatal Transmission of HIV and Board on Children, Youth, and Families (U.S.)
1999, ISBN 9780309062862, xiii, 397
Prevention | AIDS (Disease) in infants | HIV infections | Treatment | AIDS (Disease) in women | AIDS (Disease) in pregnancy
Book
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6. Born and made
: an ethnography of preimplantation genetic diagnosis
by Franklin, Sarah, 1960 and Roberts, Celia, 1968
2006, STU - Student edition, In-formation series, ISBN 9780691121925, xxii, 256
Preimplantation genetic diagnosis | Preimplantation Diagnosis | Genetic Diseases, Inborn | diagnosis | Moral and ethical aspects | Social aspects | ethics | Mfn | Sociology | General | Genetics | Medical | Social Science | Jhba | Great Britain | Health Sciences | SOCIAL SCIENCE | MEDICAL
Book
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7. A companion to bioethics
by Kuhse, Helga and Singer, Peter, 1946
1998, Blackwell companions to philosophy., ISBN 0631197370, xv, 512
Bioethics | Medical ethics
Book
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8. Full Text Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis
by Wapner, Ronald J and Martin, Christa Lese and Levy, Brynn and Ballif, Blake C and Eng, Christine M and Zachary, Julia M and Savage, Melissa and Platt, Lawrence D and Saltzman, Daniel and Grobman, William A and Klugman, Susan and Scholl, Thomas and Simpson, Joe Leigh and McCall, Kimberly and Aggarwal, Vimla S and Bunke, Brian and Nahum, Odelia and Patel, Ankita and Lamb, Allen N and Thom, Elizabeth A and Beaudet, Arthur L and Ledbetter, David H and Shaffer, Lisa G and Jackson, Laird
The New England journal of medicine, ISSN 0028-4793, 12/2012, Volume 367, Issue 23, pp. 2175 - 2184
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Biological and medical sciences | General aspects | Medical sciences | Fetal Diseases - diagnosis | Oligonucleotide Array Sequence Analysis | Chromosomes, Human - genetics | Humans | Genetic Testing - methods | Pregnancy | Maternal Age | Ultrasonography, Prenatal | Karyotyping | Chromosome Aberrations | Chromosome Disorders - diagnosis | Adult | Female | Down Syndrome - diagnosis | Prenatal Diagnosis - methods | Karyotype | Usage | DNA microarrays | Prenatal diagnosis | Diagnosis | Research | Comparative analysis | Developmental delay | Health aspects | Methods | Fetuses | Genes | Tissue culture | Prenatal development | Genomes | Medical diagnosis | Autism | Chromosome translocations | Down's syndrome | Ultrasonography | Children | Triploidy | Chromosomes | Index Medicus | Abridged Index Medicus
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9. Full Text Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: Clinical laboratory analysis of >72 400 specimens
by Sugarman, Elaine A and Nagan, Narasimhan and Zhu, Hui and Akmaev, Viatcheslav R and Zhou, Zhaoqing and Rohlfs, Elizabeth M and Flynn, Kerry and Hendrickson, Brant C and Scholl, Thomas and Sirko-Osadsa, Deborah Alexa and Allitto, Bernice A
European journal of human genetics : EJHG, ISSN 1018-4813, 01/2012, Volume 20, Issue 1, pp. 27 - 32
pan-ethnic | carrier screening | SMN1 | spinal muscular atrophy (SMA) | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Neurology | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Muscular Atrophy, Spinal - diagnosis | United States - epidemiology | Humans | Male | Genetic Counseling | Genetic Testing - methods | Genetic Carrier Screening - methods | DNA Copy Number Variations | Muscular Atrophy, Spinal - genetics | Ethnic Groups - genetics | Survival of Motor Neuron 1 Protein - genetics | Adult | Female | Prenatal Diagnosis - statistics & numerical data | Reproducibility of Results | United States - ethnology | Genetic Testing - standards | Muscular Atrophy, Spinal - ethnology | Gene Frequency | Muscular Atrophy, Spinal - epidemiology | Genotype | Sequence Analysis, DNA | Fetus - cytology | Prenatal Diagnosis - standards | Mutation | Prenatal Diagnosis - methods | Laboratories | Families & family life | Cystic fibrosis | Family medical history | Minority & ethnic groups | Population genetics | Genetic screening | Hereditary diseases | Spinal muscular atrophy | Ethnicity | Prenatal diagnosis | Genetic counseling | Gene frequency | Alleles | Ethnic groups | Fibrosis | Population | Genetics | Quantitative analysis | Index Medicus
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