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1

1951-, Miller Suzanne M., ed. Individuals, families, and the new era of genetics: Biopsychosocial perspectives. W.W. Norton, 2006.

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2

Neale, Michael C., and Lon R. Cardon. Methodology for Genetic Studies of Twins and Families. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-015-8018-2.

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3

Neale, Michael C. Methodology for genetic studies of twins and families. Kluwer Academic Publishers, 1992.

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4

Antebi, Yael Jennifer. Genetic predisoposition to ovarian cancer in Ashenazi Jewish families. National Library of Canada, 1998.

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5

Cunningham, James C. An introduction to cystic fibrosis for patients and families. 4th ed. Cystic Fibrosis Foundation, 1999.

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6

Cunningham, James C. An introduction to cystic fibrosis for patients and families. 5th ed. Cystic Fibrosis Foundation, 2003.

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7

Patenaude, Andrea Farkas. Genetic testing for cancer: Psychological approaches for helping patients and families. American Psychological Association, 2005. http://dx.doi.org/10.1037/10828-000.

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8

National Cancer Institute (U.S.). Clinical Genetics Branch. Inherited bone marrow failure syndromes: Studying families with rare blood disorders and risk of cancer. U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Cancer Institute, Division of Cancer Epidemiology and Genetics, Clinical Genetics Branch, 2002.

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9

Sneed, David. Understanding your family chemistry: How your genetic blueprint and family history affect your temperament, emotions, and health. Servant Publications, 1992.

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10

Neary, Wanda Janetta. A clinical, genetic and audiological study of patients and families with unilateral vestibular schwannomas. University of Manchester, 1995.

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11

Nerby, Jill Ann. Aniridia and WAGR syndrome: A guide for patients and families. Oxford University Press, 2010.

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12

Nerby, Jill Ann. Aniridia and WAGR syndrome: A guide for patients and families. Oxford University Press, 2010.

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13

Ann, Nerby Jill, and Otis Jessica J, eds. Aniridia and WAGR syndrome: A practical guide for patients and families. Oxford ; New York, 2009.

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14

Goshgarian, Gary. Rough beast: A novel. D.I. Fine, 1995.

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15

Ann, Nerby Jill, and Otis Jessica J, eds. Aniridia and WAGR syndrome: A guide for patients and families. Oxford ; New York, 2009.

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16

L, Gaff Clara, and Bylund Carma L, eds. Family communication about genetics: Theory and practice. Oxford University Press, 2010.

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17

Gertrud, Beck-Mannagetta, ed. Genetics of the epilepsies. Springer-Verlag, 1989.

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18

Hehl, F. J. Von der Herkunftsfamilie zur Paartherapie: Die Abhängigkeit zwischen frühen familiären Erfahrungen und späteren Beziehungsproblemen. Asanger, 2002.

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19

W, Weber, Mulvihill John J. 1943-, and Narod Steven A, eds. Familial cancer management. CRC Press, 1996.

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20

Katie, Featherstone, ed. Risky relations: Family, kinship and the new genetics. Berg, 2006.

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21

National Cancer Institute (U.S.) and Community Clinical Oncology Program (National Cancer Institute (U.S.)), eds. Concise handbook of familial cancer susceptibility syndromes. 2nd ed. Oxford University Press, 2008.

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22

Y, Barakat Amin, ed. The Kidney in genetic disease. Churchill Livingstone, 1986.

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23

Y, Barakat Amin, ed. The Kidneyin genetic disease. Churchill Livingstone, 1986.

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24

K, Chaganti R. S., and German James, eds. Genetics in clinical oncology. Oxford University Press, 1985.

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25

International Research Conference on Familial Cancer (2nd 1995 Basel, Switzerland). Hereditary cancer: Second International Research Conference on Familial Cancer, Basel, September 11-15, 1995. Edited by Müller Hj, Scott R. J, and Weber W. Karger, 1996.

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26

Honig, George R. Human hemoglobin genetics. Springer-Verlag, 1985.

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27

Gary, Miner, ed. Familial Alzheimer's disease: Molecular genetics and clinical perspectives. M. Dekker, 1989.

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28

1937-, Cruse Julius M., and Lewis R. E. 1947-, eds. Genetic basis of autoimmune disease. Karger, 1988.

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29

1931-, Tsuang Ming T., and Simpson John C, eds. Nosology, epidemiology, and genetics of schizophrenia. Elsevier, 1988.

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30

(Editor), Suzanne M. Miller, Susan H. McDaniel (Editor), John S. Rolland (Editor), and Suzanne L. Feetham (Editor), eds. Individuals, Families, and the New Era of Genetics: Biopsychosocial Perspectives. W. W. Norton, 2006.

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31

(Editor), Suzanne M. Miller, Susan H. McDaniel (Editor), John S. Rolland (Editor), and Suzanne L. Feetham (Editor), eds. Individuals, Families, and the New Era of Genetics: Biopsychosocial Perspectives. W. W. Norton, 2006.

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32

Ruland, Jeanne, and Shantidevi. Ancestral Healing for Your Spiritual and Genetic Families. Inner Traditions International, Limited, 2020.

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33

Ruland, Jeanne, and Shantidevi. Ancestral Healing for Your Spiritual and Genetic Families. Inner Traditions International, Limited, 2020.

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34

Cardon, L. R., and M. Neale. Methodology for Genetic Studies of Twins and Families. Springer London, Limited, 2013.

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35

Neale, Michael G., and Lon R. Cardon. Methodology for Genetic Studies of Twins and Families. Springer Netherlands, 2010.

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36

Cardon, L. R., and M. Neale. Methodology for Genetic Studies of Twins and Families. Springer, 2014.

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37

Moeen, Nabeeha, Masroor Elahi Babar, and Maria Arshad. Myopia : Clinical and Genetic Approach: Clinical and Genetic Study of Myopia in Myopic Families from Lahore. VDM Verlag Dr. Müller, 2011.

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38

(Foreword), Francis S. Collins, ed. Genetic Testing For Cancer: Psychological Approaches for Helping Patients and Families. American Psychological Association (APA), 2004.

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39

Sybert, Virginia P. Genetic Skin Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190276478.001.0001.

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This book is a readable, reliable guide to the diagnosis and differential of inherited skin disorders to which generalists, paediatricians, dermatologists, and geneticists can refer during an examination. The new edition reflects the most up-to-date understanding of the molecular and genetic bases of heritable skin diseases. Each chapter describes the signs and symptoms of heritable skin diseases and enumerates pertinent associated clinical features and differential diagnoses. Non-dermatological signs are symptoms round out the information on each condition. Where appropriate, descriptions of
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40

Purcell, Shaun M. Genetic Methodologies and Applications. Edited by Dennis S. Charney, Eric J. Nestler, Pamela Sklar, and Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0001.

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Mental illness is highly heritable, yet it has been difficult historically to identify the specific genes that comprise that risk. This difficulty resides in the fact that the genetic risk for all common mental disorders is polygenic, with perhaps hundreds of genetic variations, each of small effect, contributing to the overall risk. Despite these challenges, the field has made dramatic advances over the past decade in beginning to understand the genetic basis of mental illness. This chapter provides an overview of the experimental approaches used, beginning with epidemiology and population ge
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41

Deboeck, Guido. Flemish DNA & Ancestry: History of three families over five centuries using conventional and genetic genealogy. 2nd ed. Dokus Publishing, 2007.

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42

MacLeod, Rhona, and Aad Tibben. Genetic Counseling and Testing. Oxford University Press, 2014. http://dx.doi.org/10.1093/med/9780199929146.003.0008.

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This chapter considers the challenges for clinicians involved in genetic counseling for Huntington’s disease, referring to the literature and best-practice guidelines. The issues involved in genetic testing and counseling around reproductive options are discussed. Ways of tailoring predictive test counseling to take better account of individuals’ experiences and knowledge are explored, and more complex predictive test counseling scenarios, such as requests from minors and individuals at 25% risk, are also covered. The process of assisting families near the time of diagnosis is explored, includ
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43

Random Families: Genetic Strangers, Sperm Donor Siblings, and the Creation of New Kin. Oxford University Press, Incorporated, 2018.

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44

Hertz, Rosanna, and Margaret K. Nelson. Random Families: Genetic Strangers, Sperm Donor Siblings, and the Creation of New Kin. Oxford University Press, Incorporated, 2020.

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45

Hertz, Rosanna, and Margaret K. Nelson. Random Families: Genetic Strangers, Sperm Donor Siblings, and the Creation of New Kin. Oxford University Press, Incorporated, 2018.

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46

Spana, Jacob. Lung Disease Guidelines : Background about Lung for Patients, Families, and Caregivers: Lung Diseases Genetic. Independently Published, 2021.

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47

DeMaria, Rita, Gerald R. Weeks, and Markie L. C. Twist. Focused Genograms: Intergenerational Assessment of Individuals, Couples, and Families. Taylor & Francis Group, 2017.

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48

DeMaria, Rita, Gerald R. Weeks, and Markie L. C. Twist. Focused Genograms: Intergenerational Assessment of Individuals, Couples, and Families. Taylor & Francis Group, 2017.

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49

DeMaria, Rita. Focused Genograms: Intergenerational Assessment of Individuals, Couples, and Families. Taylor & Francis Group, 2013.

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50

Distel, Marijn A., and Marleen H. M. de Moor. Genetic Influences on Borderline Personality Disorder. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199997510.003.0007.

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Borderline personality disorder (BPD) tends to “run in families.” Twin and twin family studies show that BPD is moderately heritable, with some evidence for nonadditive gene action. BPD co-occurs with Axis I and other Axis II disorders, as well as with a certain profile of normal personality traits. Multivariate twin (family) studies have shown that these phenotypic associations are partly due to genetic associations, and this is observed most strongly for BPD and neuroticism. Candidate gene-finding studies for BPD suggest the possible role of genes in the serotonergic and dopaminergic system,
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