Chromosomal abnormalities / / Tulay Askin Celik, Subrata Dey, editors |
Pubbl/distr/stampa | [Place of publication not identified] : , : IntechOpen, , [2020] |
Descrizione fisica | 1 online resource (166 pages) : illustrations |
Disciplina | 616.042 |
Soggetto topico | Human chromosome abnormalities |
ISBN | 1-78985-980-8 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910431359503321 |
[Place of publication not identified] : , : IntechOpen, , [2020] | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Genetic testing [[electronic resource] ] : care, consent, and liability / / Neil F. Sharpe, Ronald F. Carter |
Autore | Sharpe Neil F |
Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Liss, c2006 |
Descrizione fisica | 1 online resource (622 p.) |
Disciplina |
616.042
616/.042 |
Altri autori (Persone) | CarterRonald F |
Soggetto topico | Human chromosome abnormalities |
Soggetto genere / forma | Electronic books. |
ISBN |
1-280-28812-4
9786610288120 0-470-36082-8 0-471-74889-7 0-471-74888-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Genetic Testing; Contents; Contributors; Foreword; 1 Genetic Counseling and the Physician-Patient Relationship; Overview; Introduction; Core Concepts; Trust, Genetic Testing, and the Physician-Patient Relationship; Genetic Counseling and the Physician-Patient Relationship; Nondirectiveness; Web Resources; Genetic Counseling Approach to Genetic Testing; Introduction to Genetic Counseling; Historical Perspective and the Role of Nondirectiveness in Genetic Counseling; Practice of Genetic Counseling Today; Genetic Counselor Goals; Important Cultural Considerations in Genetic Counseling
Factors That Promote Effective Genetic CounselingGenetics in Mainstream Medical Care: The Emerging Milieu; Categories of Genetic Testing: Issues to Consider; Summary; 2 Communication; Overview; Need To Know; Standards; Watch Out For; Obligations; Methods; Terms, Tone, and Follow-up; Culture and Communication in the Realm of Fetal Diagnosis: Unique Considerations for Latino Patients; Miscommunication and Prenatal Genetic Care; Idioms and Jargon; Suggestions; Cultural Sensitivity; Genetic Consultation; Opportunistic Observation; Translation and Second-Hand Information; On-Site Translators Genetic ConsultationInterview after Consultation; Family and Friends as Translators; Confidence and Trust; Woman Who Declined Amniocentesis; Woman Who Accepted Amniocentesis; Discussion: Communication, Miscommunication, and Genetic Counseling; Conclusion; Communication: Clinical Diagnosis; History; Background and Diagnostic Criteria for NF1; Molecular Genetics; Issues; Introduction; Client Characteristics: Culture and Intellect; Educational Tools and Facilitators; Decision Making: Considerations and Approaches; 3 Psychological Aspects; Overview; Introduction; Scenario 1; Scenario 2 Need to KnowPotential for Psychological Harm; Potential for Psychological Benefit; Anxiety and Perceived Risk: Pretest Status of Patient; Recognizing Psychological Stress; Coping with Stress Induced by Genetic Counseling and Testing; Watch Out For; Factors Affecting Perception; Standards and Interpretation; Psychological Aspects of Genetic Testing For Adult-Onset Hereditary Disorders; Introduction; Process of Genetic Testing; Pretest Genetic Counseling Phase; Posttest Counseling Phase: Disclosure of the Genetic Test Result; Test Result Indicating Presence of Genetic Mutation Negative Test Result Indicating Absence of Genetic MutationReceiving an Ambiguous Genetic Test Result; Impact of Genetic Testing on the Family; Societal and Ethical Issues Linked to Psychosocial Outcomes; Clinical Implications; Summary; 4 Duty of Care; Overview; Need to Know; Standard of Care; Watch Out For; Duty of Care; 5 Family History; Overview; Introduction; Clinical Scenario; Need to Know; Family Pedigree; Watch Out For; Inaccurate or Incomplete Information; Prenatal and Neonatal Testing; Family History in Adult-Onset Disorders Importance of Family History in Approaches to Common Chronic Diseases of Adulthood |
Record Nr. | UNINA-9910143565603321 |
Sharpe Neil F | ||
Hoboken, N.J., : Wiley-Liss, c2006 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Genetic testing [[electronic resource] ] : care, consent, and liability / / Neil F. Sharpe, Ronald F. Carter |
Autore | Sharpe Neil F |
Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Liss, c2006 |
Descrizione fisica | 1 online resource (622 p.) |
Disciplina |
616.042
616/.042 |
Altri autori (Persone) | CarterRonald F |
Soggetto topico | Human chromosome abnormalities |
ISBN |
1-280-28812-4
9786610288120 0-470-36082-8 0-471-74889-7 0-471-74888-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Genetic Testing; Contents; Contributors; Foreword; 1 Genetic Counseling and the Physician-Patient Relationship; Overview; Introduction; Core Concepts; Trust, Genetic Testing, and the Physician-Patient Relationship; Genetic Counseling and the Physician-Patient Relationship; Nondirectiveness; Web Resources; Genetic Counseling Approach to Genetic Testing; Introduction to Genetic Counseling; Historical Perspective and the Role of Nondirectiveness in Genetic Counseling; Practice of Genetic Counseling Today; Genetic Counselor Goals; Important Cultural Considerations in Genetic Counseling
Factors That Promote Effective Genetic CounselingGenetics in Mainstream Medical Care: The Emerging Milieu; Categories of Genetic Testing: Issues to Consider; Summary; 2 Communication; Overview; Need To Know; Standards; Watch Out For; Obligations; Methods; Terms, Tone, and Follow-up; Culture and Communication in the Realm of Fetal Diagnosis: Unique Considerations for Latino Patients; Miscommunication and Prenatal Genetic Care; Idioms and Jargon; Suggestions; Cultural Sensitivity; Genetic Consultation; Opportunistic Observation; Translation and Second-Hand Information; On-Site Translators Genetic ConsultationInterview after Consultation; Family and Friends as Translators; Confidence and Trust; Woman Who Declined Amniocentesis; Woman Who Accepted Amniocentesis; Discussion: Communication, Miscommunication, and Genetic Counseling; Conclusion; Communication: Clinical Diagnosis; History; Background and Diagnostic Criteria for NF1; Molecular Genetics; Issues; Introduction; Client Characteristics: Culture and Intellect; Educational Tools and Facilitators; Decision Making: Considerations and Approaches; 3 Psychological Aspects; Overview; Introduction; Scenario 1; Scenario 2 Need to KnowPotential for Psychological Harm; Potential for Psychological Benefit; Anxiety and Perceived Risk: Pretest Status of Patient; Recognizing Psychological Stress; Coping with Stress Induced by Genetic Counseling and Testing; Watch Out For; Factors Affecting Perception; Standards and Interpretation; Psychological Aspects of Genetic Testing For Adult-Onset Hereditary Disorders; Introduction; Process of Genetic Testing; Pretest Genetic Counseling Phase; Posttest Counseling Phase: Disclosure of the Genetic Test Result; Test Result Indicating Presence of Genetic Mutation Negative Test Result Indicating Absence of Genetic MutationReceiving an Ambiguous Genetic Test Result; Impact of Genetic Testing on the Family; Societal and Ethical Issues Linked to Psychosocial Outcomes; Clinical Implications; Summary; 4 Duty of Care; Overview; Need to Know; Standard of Care; Watch Out For; Duty of Care; 5 Family History; Overview; Introduction; Clinical Scenario; Need to Know; Family Pedigree; Watch Out For; Inaccurate or Incomplete Information; Prenatal and Neonatal Testing; Family History in Adult-Onset Disorders Importance of Family History in Approaches to Common Chronic Diseases of Adulthood |
Record Nr. | UNINA-9910830181503321 |
Sharpe Neil F | ||
Hoboken, N.J., : Wiley-Liss, c2006 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Genetic testing [[electronic resource] ] : care, consent, and liability / / Neil F. Sharpe, Ronald F. Carter |
Autore | Sharpe Neil F |
Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Liss, c2006 |
Descrizione fisica | 1 online resource (622 p.) |
Disciplina |
616.042
616/.042 |
Altri autori (Persone) | CarterRonald F |
Soggetto topico | Human chromosome abnormalities |
ISBN |
1-280-28812-4
9786610288120 0-470-36082-8 0-471-74889-7 0-471-74888-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Genetic Testing; Contents; Contributors; Foreword; 1 Genetic Counseling and the Physician-Patient Relationship; Overview; Introduction; Core Concepts; Trust, Genetic Testing, and the Physician-Patient Relationship; Genetic Counseling and the Physician-Patient Relationship; Nondirectiveness; Web Resources; Genetic Counseling Approach to Genetic Testing; Introduction to Genetic Counseling; Historical Perspective and the Role of Nondirectiveness in Genetic Counseling; Practice of Genetic Counseling Today; Genetic Counselor Goals; Important Cultural Considerations in Genetic Counseling
Factors That Promote Effective Genetic CounselingGenetics in Mainstream Medical Care: The Emerging Milieu; Categories of Genetic Testing: Issues to Consider; Summary; 2 Communication; Overview; Need To Know; Standards; Watch Out For; Obligations; Methods; Terms, Tone, and Follow-up; Culture and Communication in the Realm of Fetal Diagnosis: Unique Considerations for Latino Patients; Miscommunication and Prenatal Genetic Care; Idioms and Jargon; Suggestions; Cultural Sensitivity; Genetic Consultation; Opportunistic Observation; Translation and Second-Hand Information; On-Site Translators Genetic ConsultationInterview after Consultation; Family and Friends as Translators; Confidence and Trust; Woman Who Declined Amniocentesis; Woman Who Accepted Amniocentesis; Discussion: Communication, Miscommunication, and Genetic Counseling; Conclusion; Communication: Clinical Diagnosis; History; Background and Diagnostic Criteria for NF1; Molecular Genetics; Issues; Introduction; Client Characteristics: Culture and Intellect; Educational Tools and Facilitators; Decision Making: Considerations and Approaches; 3 Psychological Aspects; Overview; Introduction; Scenario 1; Scenario 2 Need to KnowPotential for Psychological Harm; Potential for Psychological Benefit; Anxiety and Perceived Risk: Pretest Status of Patient; Recognizing Psychological Stress; Coping with Stress Induced by Genetic Counseling and Testing; Watch Out For; Factors Affecting Perception; Standards and Interpretation; Psychological Aspects of Genetic Testing For Adult-Onset Hereditary Disorders; Introduction; Process of Genetic Testing; Pretest Genetic Counseling Phase; Posttest Counseling Phase: Disclosure of the Genetic Test Result; Test Result Indicating Presence of Genetic Mutation Negative Test Result Indicating Absence of Genetic MutationReceiving an Ambiguous Genetic Test Result; Impact of Genetic Testing on the Family; Societal and Ethical Issues Linked to Psychosocial Outcomes; Clinical Implications; Summary; 4 Duty of Care; Overview; Need to Know; Standard of Care; Watch Out For; Duty of Care; 5 Family History; Overview; Introduction; Clinical Scenario; Need to Know; Family Pedigree; Watch Out For; Inaccurate or Incomplete Information; Prenatal and Neonatal Testing; Family History in Adult-Onset Disorders Importance of Family History in Approaches to Common Chronic Diseases of Adulthood |
Record Nr. | UNINA-9910841759903321 |
Sharpe Neil F | ||
Hoboken, N.J., : Wiley-Liss, c2006 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Human molecular genetics |
Pubbl/distr/stampa | Oxford, : Oxford University Press |
Disciplina | 611.01816 |
Soggetto topico |
Human molecular genetics
Human chromosome abnormalities Cytogenetics Molecular Biology Genetics, Medical Molekulargenetik Zeitschrift Online-Ressource |
Soggetto genere / forma | Periodicals. |
ISSN | 1460-2083 |
Formato | Materiale a stampa |
Livello bibliografico | Periodico |
Lingua di pubblicazione | eng |
Altri titoli varianti | HMG |
Record Nr. | UNISA-996199891303316 |
Oxford, : Oxford University Press | ||
Materiale a stampa | ||
Lo trovi qui: Univ. di Salerno | ||
|
Human molecular genetics |
Pubbl/distr/stampa | Oxford, : Oxford University Press |
Disciplina | 611.01816 |
Soggetto topico |
Human molecular genetics
Human chromosome abnormalities Cytogenetics Molecular Biology Genetics, Medical Molekulargenetik Zeitschrift Online-Ressource |
Soggetto genere / forma | Periodicals. |
ISSN | 1460-2083 |
Formato | Materiale a stampa |
Livello bibliografico | Periodico |
Lingua di pubblicazione | eng |
Altri titoli varianti | HMG |
Record Nr. | UNINA-9910143002403321 |
Oxford, : Oxford University Press | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Human mutation |
Pubbl/distr/stampa | [New York, N.Y.], : Wiley-Liss, Inc., ©1992- |
Disciplina | 616 |
Soggetto topico |
Human chromosome abnormalities
Mutation (Biology) Medical genetics - Periodicals Medical genetics Mutation - genetics Genetics, Medical Génétique médicale - Périodiques Chromosomes humains - Anomalies Mutation (Biologie) Génétique médicale |
Soggetto genere / forma | Periodicals. |
ISSN | 1098-1004 |
Formato | Materiale a stampa |
Livello bibliografico | Periodico |
Lingua di pubblicazione | eng |
Record Nr. | UNISA-996198572203316 |
[New York, N.Y.], : Wiley-Liss, Inc., ©1992- | ||
Materiale a stampa | ||
Lo trovi qui: Univ. di Salerno | ||
|
Human mutation |
Pubbl/distr/stampa | [New York, N.Y.], : Wiley-Liss, Inc., ©1992- |
Disciplina | 616 |
Soggetto topico |
Human chromosome abnormalities
Mutation (Biology) Medical genetics - Periodicals Medical genetics Mutation - genetics Genetics, Medical Génétique médicale - Périodiques Chromosomes humains - Anomalies Mutation (Biologie) Génétique médicale |
Soggetto genere / forma | Periodicals. |
ISSN | 1098-1004 |
Formato | Materiale a stampa |
Livello bibliografico | Periodico |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910144004103321 |
[New York, N.Y.], : Wiley-Liss, Inc., ©1992- | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Muscular and skeletal anomalies in human trisomy in an evo-devo context : description of a T18 cyclopic fetus and comparison between Edwards (T18), Patau (T13) and Down (T21) syndromes using 3-D imaging and anatomical illustrations / / Christopher M. Smith [et al.], editors |
Pubbl/distr/stampa | Boca Raton : , : CRC Press : , : Taylor & Francis Group, , [2015] |
Descrizione fisica | 1 online resource (x, 212 pages) : illustrations (some color) |
Disciplina | 618.920042 |
Soggetto topico |
Abnormalities, Human - Genetic aspects
Human chromosome abnormalities Human anatomy |
ISBN |
0-429-17333-4
1-4987-1138-3 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Front Cover; Preface; Acknowledgements; Contents; Chapter 1 - Topics and Purpose of this Book; Chapter 2 - The Musculoskeletal System of a 28-week Human Trisomy 18 Cyclopia Fetus; Chapter 3 - Comparative Anatomy of Muscular Anomalies in Trisomies 13, 18, and 21; Chapter 4 - Cyclopia, Trisomic Anomalies, and Order versus Chaos in Development and Evolution; Chapter 5 - Digits and Muscles: Topology-Directed Muscle Attachment; Chapter 6 - Evolutionary Mechanisms and Mouse Models for Down Syndrome; Illustrations; References; Appendix A - Dissection Photographs of Trisomy 18 Human Cyclopia Fetus; Appendix B - 3-D Renders of Trisomy 18 Human Cyclopia Fetus CT Scan Data; About the Authors; Color Plate Section; Back Cover |
Record Nr. | UNINA-9910787342203321 |
Boca Raton : , : CRC Press : , : Taylor & Francis Group, , [2015] | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Muscular and skeletal anomalies in human trisomy in an evo-devo context : description of a T18 cyclopic fetus and comparison between Edwards (T18), Patau (T13) and Down (T21) syndromes using 3-D imaging and anatomical illustrations / / Christopher M. Smith [et al.], editors |
Edizione | [1st ed.] |
Pubbl/distr/stampa | Boca Raton : , : CRC Press : , : Taylor & Francis Group, , [2015] |
Descrizione fisica | 1 online resource (x, 212 pages) : illustrations (some color) |
Disciplina | 618.920042 |
Soggetto topico |
Abnormalities, Human - Genetic aspects
Human chromosome abnormalities Human anatomy |
ISBN |
0-429-17333-4
1-4987-1138-3 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Front Cover; Preface; Acknowledgements; Contents; Chapter 1 - Topics and Purpose of this Book; Chapter 2 - The Musculoskeletal System of a 28-week Human Trisomy 18 Cyclopia Fetus; Chapter 3 - Comparative Anatomy of Muscular Anomalies in Trisomies 13, 18, and 21; Chapter 4 - Cyclopia, Trisomic Anomalies, and Order versus Chaos in Development and Evolution; Chapter 5 - Digits and Muscles: Topology-Directed Muscle Attachment; Chapter 6 - Evolutionary Mechanisms and Mouse Models for Down Syndrome; Illustrations; References; Appendix A - Dissection Photographs of Trisomy 18 Human Cyclopia Fetus; Appendix B - 3-D Renders of Trisomy 18 Human Cyclopia Fetus CT Scan Data; About the Authors; Color Plate Section; Back Cover |
Record Nr. | UNINA-9910807969703321 |
Boca Raton : , : CRC Press : , : Taylor & Francis Group, , [2015] | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|