Tesis sobre el tema "Genetic counseling"
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Reis, Linda M. "Spiritual Assessment in Genetic Counseling". University of Cincinnati / OhioLINK, 2004. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1090644974.
Texto completoBarnett, Chloe. "The Gendered Pay Gap in Genetic Counseling". University of Cincinnati / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1583998580304134.
Texto completoSomers, Allyson. "Provision of cardiovascular genetic counseling services: current practice and future directions". University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367924189.
Texto completoWilliams, Misti D. "Collaborative Partnerships Between Genetic Counselors and Genetic Advocacy/Support Groups: The Genetic Counseling Perspective". Cincinnati, Ohio : University of Cincinnati, 2006. http://rave.ohiolink.edu/etdc//view?acc_num=ucin1151510578.
Texto completoAdvisor: Nancy Steinberg Warren. Title from electronic thesis title page (viewed July 17, 2009). Includes abstract. Keywords: Genetic advocacy, professional collaborations, genetic counseling, genetic; conditions, support groups. Includes bibliographical references.
Salmon, Anderson Tricia. "Sickle Cell Trait and Genetic Counseling". ScholarWorks, 2017. https://scholarworks.waldenu.edu/dissertations/4020.
Texto completoWallace, Jody P. "Employability of Genetic Counselors with a PhD in Genetic Counseling". University of Cincinnati / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1179428260.
Texto completoMarbach, Rachel. "The frequency of spontaneously reported psychiatric disorders on pre-genetic counseling appointment intake forms and during counseling sessions". The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu158688292193696.
Texto completoPsensky, Brittany. "Factors Impacting Attendance of Patients with HCM for Cardiovascular Genetic Counseling". Case Western Reserve University School of Graduate Studies / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=case1339083273.
Texto completoLahner, Nicole. "Assessment of Genetic Provider and Parent Communication Patterns in Pediatric Genetic Counseling Sessions". The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1460379299.
Texto completoLewis, Courtney. "Genetics Laboratory Directors’ Perspectives on the Role of Genetic Counselors in Acquired Mutation Testing: Current and Expanded Opportunities". University of Cincinnati / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396523134.
Texto completoHayat, Roshanai Afsaneh. "Psychological and Behavioral Aspects of Receiving Genetic Counseling for Hereditary Cancer". Doctoral thesis, Uppsala universitet, Vårdvetenskap, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-128870.
Texto completoCzape, Kayla. "Parent preferences regarding educational material and genetic counseling for hearing loss genetic testing". University of Cincinnati / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1276974727.
Texto completoPeplow, Katherine. "Discussions of Personal Identity in Genetic Counseling Supervision". University of Cincinnati / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1623165916484682.
Texto completoFreeze, Samantha. "Genetic Testing and Counseling Practices for Patients with Retinoblastoma at Cincinnati Children’s Hospital Medical Center". University of Cincinnati / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1427813631.
Texto completoUsrey, Kelly Marie. "Complementary and alternativve medicine in genetic counseling". Oklahoma City : [s.n.], 2010.
Buscar texto completoSmith, Jenny. "Impact of the word "counseling" on likelihood to schedule an appointment for genetic counseling". Cincinnati, Ohio : University of Cincinnati, 2005. http://www.ohiolink.edu/etd/view.cgi?acc%5Fnum=ucin1123171118.
Texto completoTitle from electronic thesis title page (viewed Feb. 25, 2006). Includes abstract. Keywords: genetic counseling, genetic risk assessment, referral terminology, attitude, barriers. Includes bibliographical references.
Masunga, Abigail N. "Barriers Impacting the Utilization of Supervision Techniques in Genetic Counseling". University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367919500.
Texto completoDeeney, Meghan. "Beginning genetic counselors' comfort level with grief and loss in the clinical setting". Waltham, Mass. : Brandeis University, 2009. http://dcoll.brandeis.edu/handle/10192/23241.
Texto completoSerra, Juhé Clara 1984. "Genetic, genomic and epigenetic alterations in congenital malformations : implications in genetic counseling". Doctoral thesis, Universitat Pompeu Fabra, 2012. http://hdl.handle.net/10803/96194.
Texto completoEls mecanismes causants de les malformacions congènites són poc coneguts malgrat l’elevada incidència d’aquestes patologies, que afecten el 2-3% de recent nascuts. Un coneixement més ampli de les causes de les anomalies congènites proporcionaria informació rellevant pel que fa al pronòstic de l’anomalia, el desenvolupament i establiment de protocols diagnòstics, el disseny d’estratègies terapèutiques, així com l’assessorament genètic a la família. En la tesi que es presenta s’han utilitzat diferents estratègies, pel que fa a tecnologies i models de malalties, amb l’objectiu d’esbrinar la contribució d’alteracions genètiques i epigenètiques en l’etiopatogènia de les malformacions congènites. S’han analitzat variacions en número de còpia, patrons de metilació, així com mutacions puntuals. D’altra banda, també s’ha realitzat un estudi per aprofundir en l’assessorament genètic en relació a una de les noves tècniques moleculars utilitzades. Els resultats obtinguts indiquen que les altercacions genètiques i epigenètiques tenen una contribució molt rellevant en l’etiologia de les malformacions congènites, en alguns casos com a causa única de la malaltia i en altres com a component d’un model oligogènic o multifactorial.
Feldman, Jessica S. "How Much We Tell Our Patients: Counseling Differences between Genetic Counselors and Other Providers". University of Cincinnati / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1592135842556374.
Texto completoSmith, Marissa B. "A description of genetic counselors' views and current practice with regard to the use of array-CGH for prenatal diagnosis". Cleveland, Ohio : Case Western Reserve University, 2009. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=case1246977726.
Texto completoSchaber, Abigail Nicole. "Genetic Counseling and Testing in a Pediatric Population with Autism Spectrum Disorder (ASD)". The Ohio State University, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu155490405885201.
Texto completoWinslow, Hayley R. "Pre- and Post-Test Parent Perceptions of Genetic Testing for Children with Autism Spectrum Disorder (ASD)". The Ohio State University, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=osu1492505122437373.
Texto completoLee, Sansan. "Genetic counseling perspectives on prenatal array CGH testing". Waltham, Mass. : Brandeis University, 2009. http://dcoll.brandeis.edu/handle/10192/23259.
Texto completoArmstrong, Katherine B. "The Genetic Counseling Experience in a Multidisciplinary Childhood Cancer Survivor Center". University of Cincinnati / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1337101530.
Texto completoGaonkar, Shraddha. "Challenges in counseling for rare chromosome conditions genetic counselors' perspective /". Waltham, Mass. : Brandeis University, 2009. http://dcoll.brandeis.edu/handle/10192/23239.
Texto completoCodina, i. Solà Marta 1988. "Genetic variation and complex rearrangements in Autism Spectrum Disorders: implications for genetic counseling". Doctoral thesis, Universitat Pompeu Fabra, 2016. http://hdl.handle.net/10803/388031.
Texto completoMalgrat el fort component genètic dels Trastorns de l’Espectre Autista (TEA), l’etiologia de la majoria de casos es desconeix. Un major coneixement de les seves bases genètiques seria molt beneficiós, ja que permetria un assessorament genètic específic a les famílies i, a la llarga, el desenvolupament d’estratègies terapèutiques personalitzades. En aquesta tesis, s’han aplicat diverses tècniques recents de seqüenciació i estratègies d’anàlisi adaptades. S’ha investigat el paper de variants rares i les seves conseqüències transcripcionals, així com de reordenaments complexos. A més, hem estudiat la presència de variants de susceptibilitat en un grup de persones amb síndrome de Williams, un trastorn genòmic associat a un fenotip oposat. Finalment, hem explorat el coneixement i les opinions en un grup de famílies afectades i, també, l’efecte de l’assessorament genètic. Els resultats obtinguts indiquen que, en el TEA, hi contribueixen tant mutacions altament penetrants, com variants heretades que augmenten lleugerament el risc i poden seguir tant models monogènics com oligogènics. Cada un d’aquests models contribuiria a explicar part de la variabilitat i dels casos
Lemons, Jennifer M. "“I didn’t know it existed until you called”: Protestant clergy experience and education of genetics". University of Cincinnati / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1307125947.
Texto completoMoore, Rebekah Ann. "Provision of Genetics Services: Is it Time to Embrace Social Media?" Case Western Reserve University School of Graduate Studies / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=case1404902803.
Texto completoOwens-Thomas, Elizabeth J. "Examining the Relationship Between Genetic Counseling Student Self-Efficacy and Clinical Training". University of Cincinnati / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1522165895007472.
Texto completoPoskochil, Jamie. "Neurologists’ Practices and Attitudes Regarding Genetic Testing for Alzheimer Disease". University of Cincinnati / OhioLINK, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1123729403.
Texto completoJacher, Joseph E. B. A. "Pulmonary Arterial Hypertension: Specialists’ Knowledge, Practices, and Attitudes of Genetic Testing and Genetic Counseling". University of Cincinnati / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1427797616.
Texto completoMelley, Caitlin. "Surgical fetal intervention assessing the current practices of genetic counselors /". Waltham, Mass. : Brandeis University, 2009. http://dcoll.brandeis.edu/handle/10192/23321.
Texto completoEshraghi, Marjan. "An exploration of the interplay between students' religious beliefs and their genetic counseling graduate training". Waltham, Mass. : Brandeis University, 2009. http://dcoll.brandeis.edu/handle/10192/23211.
Texto completoTurner, Adam y Adam Turner. ""Will My Baby Be Normal?": A History of Genetic Counseling in the United States, 1940-1970". Thesis, University of Oregon, 2012. http://hdl.handle.net/1794/12468.
Texto completoAult, Rachel Marie. "Pitfalls of Communication in a Genetic Counseling Session when Two Languages are Required". The Ohio State University, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=osu1492550859962531.
Texto completoGoldstein, Ellen Sara. "Estimating the Incidence of Germline Mutations in Patients with Bone and Soft Tissue Sarcoma using Clinical Tumor Sequencing". The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1592844958063832.
Texto completoSpaeth, Christine Grey. "Evidence for and Barriers to a Team-Based Approach for Genetic Services in Pediatric Healthcare Specialty Settings". University of Cincinnati / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1211913285.
Texto completoLaPan, Amy C. "Prenatal testing, birth outcomes, and views of social workers". online access from Digital Dissertation Consortium, 2005. http://libweb.cityu.edu.hk/cgi-bin/er/db/ddcdiss.pl?3202790.
Texto completoVan, Niekerk Katryn. "Knowledge and experiences of parents with children affected by Sickle Cell Disease in Cape Town". Master's thesis, University of Cape Town, 2015. http://hdl.handle.net/11427/16652.
Texto completoSickle Cell Disease (SCD) is an autosomal recessively inherited blood disorder that leads to a debilitating systemic illness. Although the disease was initially found predominantly in tropical and subtropical regions, SCD has now become a global health problem, due to migration of people from various countries with a high burden thereof. Consequently, the incidence of SCD in South Africa has increased dramatically over the last decade. This study, which constitutes a minor dissertation in fulfilment of an MSc (Med) Genetic Counselling degree, aimed to explore the knowledge and understanding of SCD among parents of affected children in Cape Town as well as identify burdens associated with caring for a child with SCD. Furthermore, the study assessed opportunities to improve genetic counselling services available to parents and explored their attitude to preventive policies. A phenomenological approach was used to conduct this research. Seventeen semi-structured interviews were conducted with the biological parent of a child attending the Red Cross War Memorial Children's Hospital Haematology Clinic. Participants were selected using both purposive and convenience sampling methods. Data collected during these interviews were analysed using thematic content analysis. Themes and relevant sub-themes were identified and grouped into three categories: knowledge and understanding; experiences and burdens; and attitude toward preventative policies. While the majority of participants had some knowledge of SCD, several misconceptions were discovered, often relating to participants' prior knowledge of the disease. A number of burdens experienced by participants were revealed, with both practical and psychosocial implications. Finally, it was found that the majority of participants supported all methods of screening for SCD, regardless of whether they would make use of the screening services themselves. Findings of this study provide valuable insights on the subject of experiences of parents of children affected with SCD as well as the potential role of genetic counselling services. This study contributes towards improving understanding and subsequent services provided to individuals raising a child affected with Sickle Cell Disease.
Francois, Sydney. "Investigating the views and experiences of Fetal Medicine Practitioners offering late termination of pregnancy in the Western Cape". Master's thesis, Faculty of Health Sciences, 2021. http://hdl.handle.net/11427/33748.
Texto completoAllsbrook, Katlin. "The Relationship Between the Supervision Role to Compassion Fatigue and Burnout in Genetic Counseling". University of Cincinnati / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1427981369.
Texto completoNardini, Monica. "Genomic Counseling in the Newborn Period: Are Genetic Counselors Ready?" Case Western Reserve University School of Graduate Studies / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=case1372778934.
Texto completoShuss, Christine M. "Supervisory Styles and Satisfaction: Genetic Counseling Student and Graduate Views". Case Western Reserve University School of Graduate Studies / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=case1341591706.
Texto completoByrne, Karen Elizabeth. "ANALYSIS OF PATIENTS' REACTIONS TO GENETIC COUNSELING SERVICES FOR AMNIOCENTESIS AND GENETIC DISORDERS (VIDEOTAPE PROGRAM, FOLLOW-UP LETTERS, MATERNAL AGE)". Thesis, The University of Arizona, 1985. http://hdl.handle.net/10150/275301.
Texto completoJames, Delores C. S. "A survey of genetic counseling professionals in the southeastern United States actual versus perceived roles /". Gainesville, FL, 1993. http://www.archive.org/details/surveyofgeneticc00jame.
Texto completoKelly, Anke. "Multicultural genetic counseling with Alaska native and Canadian first nations clients". Waltham, Mass. : Brandeis University, 2009. http://dcoll.brandeis.edu/handle/10192/23191.
Texto completoKnyszek, Brittney Lynn. "The Impact of Visual Aids on Prenatal Genetic Counseling Session Patient Outcomes". Case Western Reserve University School of Graduate Studies / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=case1338515186.
Texto completoMuller, Reka D. "Evaluation of Clinical Practices and Needs about Variants of Uncertain Significance Results in Inherited Cardiac Arrhythmia and Inherited Cardiomyopathy Genes". Scholar Commons, 2019. https://scholarcommons.usf.edu/etd/7863.
Texto completoNightingale, Brooke Moriarty. "Development of a Genetic Testing Report Supplement for Patients with Hypertrophic Cardiomyopathy Who Receive Uninformative Results". The Ohio State University, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1523463438552511.
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