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Chromosomal abnormalities / / Tulay Askin Celik, Subrata Dey, editors
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
Opac: Controlla la disponibilità qui
Genetic testing [[electronic resource] ] : care, consent, and liability / / Neil F. Sharpe, Ronald F. Carter
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
Opac: Controlla la disponibilità qui
Genetic testing [[electronic resource] ] : care, consent, and liability / / Neil F. Sharpe, Ronald F. Carter
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
Opac: Controlla la disponibilità qui
Genetic testing [[electronic resource] ] : care, consent, and liability / / Neil F. Sharpe, Ronald F. Carter
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
Opac: Controlla la disponibilità qui
Human molecular genetics
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
Opac: Controlla la disponibilità qui
Human molecular genetics
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
Opac: Controlla la disponibilità qui
Human mutation
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
Opac: Controlla la disponibilità qui
Human mutation
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
Opac: Controlla la disponibilità qui
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
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
Opac: Controlla la disponibilità qui
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
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
Opac: Controlla la disponibilità qui