-
1
-
-
0013380520
-
Testing children for genetic status
-
report 66
-
American Medical Association Council on Ethical and Judicial Affairs. (1995). Testing children for genetic status. Code of Medical Ethics, report 66.
-
(1995)
Code of Medical Ethics
-
-
-
2
-
-
0028872836
-
Points to consider: Ethical, legal, and psychological implications of genetic testing in children and adolescents
-
American Society of Human Genetics and the American College of Medical Genetics. (1995). Points to consider: Ethical, legal, and psychological implications of genetic testing in children and adolescents. American Journal of Human Genetics, 57, 1233-1241.
-
(1995)
American Journal of Human Genetics
, vol.57
, pp. 1233-1241
-
-
-
3
-
-
0029898347
-
Psychological impact of population-based carrier testing for cystic fibrosis: 3-year follow-up
-
Axworthy, D., Brock, D. J., Bobrow, M., & Marteau, T. H. (1996). Psychological impact of population-based carrier testing for cystic fibrosis: 3-year follow-up. Lancet, 347, 1443-1444.
-
(1996)
Lancet
, vol.347
, pp. 1443-1444
-
-
Axworthy, D.1
Brock, D.J.2
Bobrow, M.3
Marteau, T.H.4
-
4
-
-
0029872978
-
Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives
-
Bailey, A., Phillips, W., & Rutter, M. (1996). Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives. Journal of Child Psychology and Psychiatry, 37, 89-126.
-
(1996)
Journal of Child Psychology and Psychiatry
, vol.37
, pp. 89-126
-
-
Bailey, A.1
Phillips, W.2
Rutter, M.3
-
5
-
-
0033647053
-
FMR1 gene and fragile X syndrome
-
Bardoni B., Mandel, J. L., & Fisch, G. S. (2000). FMR1 gene and fragile X syndrome. American Journal of Medical Genetics, 97, 153-163.
-
(2000)
American Journal of Medical Genetics
, vol.97
, pp. 153-163
-
-
Bardoni, B.1
Mandel, J.L.2
Fisch, G.S.3
-
6
-
-
0027263385
-
The impact of parental affective disorder on depression in offspring: A longitudinal follow-up in a non-referred sample
-
Beardslee, W. R., Keller, M. B., Lavori, P. W., Staley, J., & Sacks, N. (1993). The impact of parental affective disorder on depression in offspring: A longitudinal follow-up in a non-referred sample. Journal of the American Academy of Child and Adolescent Psychiatry, 32, 723-730.
-
(1993)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.32
, pp. 723-730
-
-
Beardslee, W.R.1
Keller, M.B.2
Lavori, P.W.3
Staley, J.4
Sacks, N.5
-
7
-
-
0026670872
-
Further evidence for familial-genetic risk factors in ADHD: Patterns of comorbidity in probands and relatives in psychiatrically and pediatrically referred samples
-
Biederman, J., Farone, S. V., Keenan, K., Benjamin, J., Krifcher, B., Moore, C., Sprich, S., Ugaglia, K., Jellineck, M. S., Steingard, R., Spencer, T., Norman, D., Kolodny, R., Kraus, I., Perrin, J., Keller, M. B., & Tsuang, M. (1992). Further evidence for familial-genetic risk factors in ADHD: Patterns of comorbidity in probands and relatives in psychiatrically and pediatrically referred samples. Archives of General Psychiatry, 49, 728-738.
-
(1992)
Archives of General Psychiatry
, vol.49
, pp. 728-738
-
-
Biederman, J.1
Farone, S.V.2
Keenan, K.3
Benjamin, J.4
Krifcher, B.5
Moore, C.6
Sprich, S.7
Ugaglia, K.8
Jellineck, M.S.9
Steingard, R.10
Spencer, T.11
Norman, D.12
Kolodny, R.13
Kraus, I.14
Perrin, J.15
Keller, M.B.16
Tsuang, M.17
-
10
-
-
0001539758
-
What should the law say about disclosure of genetic information to relatives?
-
Clayton, E. C. (1998). What should the law say about disclosure of genetic information to relatives? Journal of Health Care Law & Policy, 1, 373-391.
-
(1998)
Journal of Health Care Law & Policy
, vol.1
, pp. 373-391
-
-
Clayton, E.C.1
-
11
-
-
0029904635
-
Genetic testing for cancer in children: Short-term psychological effect
-
Codori, A.-M., Petersen, G., Boyd, P, Brandt, J., & Giardiello, F M. (1996). Genetic testing for cancer in children: Short-term psychological effect. Pediatrics and Adolescent Medicine, 150, 1131-1138.
-
(1996)
Pediatrics and Adolescent Medicine
, vol.150
, pp. 1131-1138
-
-
Codori, A.-M.1
Petersen, G.2
Boyd, P.3
Brandt, J.4
Giardiello, F.M.5
-
12
-
-
0000928771
-
Commentary on the ASCO statement on genetic testing for cancer susceptibility
-
Collins, F. (1996). Commentary on the ASCO statement on genetic testing for cancer susceptibility. Journal of Clinical Oncology, 14, 1738-1740.
-
(1996)
Journal of Clinical Oncology
, vol.14
, pp. 1738-1740
-
-
Collins, F.1
-
14
-
-
0035060793
-
Nuts and bolts of psychiatric genetics: Building on the Human Genome Project
-
Evans, K. L., Muir, W. J., Blackwood, D. H. R., & Porteous, D. J. (2001). Nuts and bolts of psychiatric genetics: Building on the Human Genome Project. Trends in Genetics, 17, 335-340.
-
(2001)
Trends in Genetics
, vol.17
, pp. 335-340
-
-
Evans, K.L.1
Muir, W.J.2
Blackwood, D.H.R.3
Porteous, D.J.4
-
15
-
-
0030972226
-
Developmental tasks of childhood and adolescence: Implications for genetic testing
-
Fanos, J. (1997). Developmental tasks of childhood and adolescence: implications for genetic testing. American Journal of Medical Genetics, 71, 22-28.
-
(1997)
American Journal of Medical Genetics
, vol.71
, pp. 22-28
-
-
Fanos, J.1
-
16
-
-
0003605370
-
-
New York: Guilford Press
-
Farone, S. V., Tsuang, M. T., & Tsuang, D. W. (1999). Genetics of mental disorders: A guide for students, clinicians, and researchers. New York: Guilford Press.
-
(1999)
Genetics of Mental Disorders: A Guide for Students, Clinicians, and Researchers
-
-
Farone, S.V.1
Tsuang, M.T.2
Tsuang, D.W.3
-
17
-
-
0343224712
-
The concentration of offending behavior in families
-
Farrington, D. P, Barnes, G. C., & Lambert S. (1996). The concentration of offending behavior in families. Legal and Criminological Psychology, 1, 47-63.
-
(1996)
Legal and Criminological Psychology
, vol.1
, pp. 47-63
-
-
Farrington, D.P.1
Barnes, G.C.2
Lambert, S.3
-
18
-
-
0032215197
-
The case against preadoption genetic testing
-
Freundlich, M. D. (1998). The case against preadoption genetic testing. Child Welfare, 77, 663-679.
-
(1998)
Child Welfare
, vol.77
, pp. 663-679
-
-
Freundlich, M.D.1
-
19
-
-
0028881997
-
Clinical use of molecular information in the management of multiple endocrine neoplasia type 2A
-
Gagel, R. F., Cote, G. J., Martins Bugalho, M. J., Boyd, A. E. 3rd, Cummings, T., Goepfert, H., Evans, D. B., Cangir, A., Khorana, S., & Schultz, P. N. (1995). Clinical use of molecular information in the management of multiple endocrine neoplasia type 2A. Journal of Internal Medicine, 238, 333-341.
-
(1995)
Journal of Internal Medicine
, vol.238
, pp. 333-341
-
-
Gagel, R.F.1
Cote, G.J.2
Martins Bugalho, M.J.3
Boyd A.E. III4
Cummings, T.5
Goepfert, H.6
Evans, D.B.7
Cangir, A.8
Khorana, S.9
Schultz, P.N.10
-
20
-
-
0034265307
-
Mothers and daughters from breast cancer families: A qualitative study of their perceptions of risk and benefits associated with minor's participation in genetic susceptibility research
-
Geller, G., Tambor, E. S., Bernhardt, B. A., Wissow, L. S., & Fraser, G. (2000). Mothers and daughters from breast cancer families: A qualitative study of their perceptions of risk and benefits associated with minor's participation in genetic susceptibility research. Journal of the American Medical Womens Association, 55, 280-284.
-
(2000)
Journal of the American Medical Womens Association
, vol.55
, pp. 280-284
-
-
Geller, G.1
Tambor, E.S.2
Bernhardt, B.A.3
Wissow, L.S.4
Fraser, G.5
-
21
-
-
0035746534
-
Cystic fibrosis population carrier screening: Here at last - Are we ready?
-
Grody, W. W., & Desnick, R. J. (2001). Cystic fibrosis population carrier screening: Here at last - Are we ready? Genetics in Medicine, 3, 87-90.
-
(2001)
Genetics in Medicine
, vol.3
, pp. 87-90
-
-
Grody, W.W.1
Desnick, R.J.2
-
22
-
-
0034597309
-
Parents' responses to disclosure of genetic test results of their children
-
Grosfeld, F. J. M., Beemer, F. A., Lips, C. J. M., Hendriks, K. S. W. H., & ten Kroode, H. F. J. (2000). Parents' responses to disclosure of genetic test results of their children. American Journal of Medical Genetics, 94(4), 316-323.
-
(2000)
American Journal of Medical Genetics
, vol.94
, Issue.4
, pp. 316-323
-
-
Grosfeld, F.J.M.1
Beemer, F.A.2
Lips, C.J.M.3
Hendriks, K.S.W.H.4
Ten Kroode, H.F.J.5
-
23
-
-
0034007630
-
Distress in MEN2 family members and partners prior to DNA test disclosure
-
Grosfeld, F. J. M. Lips, C. J. M., Beemer, F. A., Blijham, G. H., Quirijnen, J. M. S. P., Mastenbroek, M. P., & ten Kroode, H. F. J. (2000). Distress in MEN2 family members and partners prior to DNA test disclosure. American Journal of Medical Genetics, 91, 1-7.
-
(2000)
American Journal of Medical Genetics
, vol.91
, pp. 1-7
-
-
Grosfeld, F.J.M.1
Lips, C.J.M.2
Beemer, F.A.3
Blijham, G.H.4
Quirijnen, J.M.S.P.5
Mastenbroek, M.P.6
Ten Kroode, H.F.J.7
-
24
-
-
0034192754
-
Attitudes toward the genetic testing of children among adults in a Utah-based kindred tested for a BRCA1 mutation
-
Hamann, H., Croyle, R. T., Venne, V. L., Baty, B. J., Smith, K. R., & Botkin, J. R. (2000). Attitudes toward the genetic testing of children among adults in a Utah-based kindred tested for a BRCA1 mutation. American Journal of Medical Genetics, 92, 25-32.
-
(2000)
American Journal of Medical Genetics
, vol.92
, pp. 25-32
-
-
Hamann, H.1
Croyle, R.T.2
Venne, V.L.3
Baty, B.J.4
Smith, K.R.5
Botkin, J.R.6
-
25
-
-
0032522623
-
Multiple primary cancers in families with Li-Fraumeni syndrome
-
Hisada, M., Garber, J. E., Fung, C. Y., Fraumeni, J. F. Jr., & Li, F. P. (1998). Multiple primary cancers in families with Li-Fraumeni syndrome. Journal of the National Cancer Institute, 90, 606-611.
-
(1998)
Journal of the National Cancer Institute
, vol.90
, pp. 606-611
-
-
Hisada, M.1
Garber, J.E.2
Fung, C.Y.3
Fraumeni J.F., Jr.4
Li, F.P.5
-
27
-
-
0034234719
-
Ethical considerations in clinical pharmacogenomics research
-
Issa, A. M. (2000). Ethical considerations in clinical pharmacogenomics research. Trends in Pharmacological Sciences, 21, 247-249.
-
(2000)
Trends in Pharmacological Sciences
, vol.21
, pp. 247-249
-
-
Issa, A.M.1
-
28
-
-
18544362828
-
Recommendations of core competencies in genetics essential for all health professionals
-
Jenkins, J., Blitzer, M., Boehm, K., Feetham, S., Gettig, E., Johnson, A., Lapham, V., Patenaude, A. F., Reynolds, P., Guttmacher, A. E., & the Core Competency Working Group of the National Coalition for Health Professional Education in Genetics. (2001). Recommendations of core competencies in genetics essential for all health professionals. Genetics in Medicine, 3, 155-158.
-
(2001)
Genetics in Medicine
, vol.3
, pp. 155-158
-
-
Jenkins, J.1
Blitzer, M.2
Boehm, K.3
Feetham, S.4
Gettig, E.5
Johnson, A.6
Lapham, V.7
Patenaude, A.F.8
Reynolds, P.9
Guttmacher, A.E.10
-
29
-
-
0033984130
-
Screening children at risk of developing inherited endocrine neoplasia syndromes
-
Johnston, L. B., Chew, S. L., Trainer, P. J., Reznekt, R., Grossman, A. B., Besser, G. M., Monson, J. P., & Savage, M. O. (2000). Screening children at risk of developing inherited endocrine neoplasia syndromes. Clinical Endocrinology, 52, 127-136.
-
(2000)
Clinical Endocrinology
, vol.52
, pp. 127-136
-
-
Johnston, L.B.1
Chew, S.L.2
Trainer, P.J.3
Reznekt, R.4
Grossman, A.B.5
Besser, G.M.6
Monson, J.P.7
Savage, M.O.8
-
30
-
-
0028933970
-
Pharmaocgenetics and development: Are infants and children at increased risk for adverse outcomes?
-
Kearns, G. L. (1995). Pharmaocgenetics and development: Are infants and children at increased risk for adverse outcomes? Current Opinion in Pediatrics, 7, 220-233.
-
(1995)
Current Opinion in Pediatrics
, vol.7
, pp. 220-233
-
-
Kearns, G.L.1
-
31
-
-
0035828112
-
Tryptophan hydroxylase gene variant and smoking behavior
-
Lerman, C., Caporaso, N. E., Bush, A., Audrain, J., Main, D., & Shields, P G. (2001). Tryptophan hydroxylase gene variant and smoking behavior. American Journal of Medical Genetics, 105(6), 518-520.
-
(2001)
American Journal of Medical Genetics
, vol.105
, Issue.6
, pp. 518-520
-
-
Lerman, C.1
Caporaso, N.E.2
Bush, A.3
Audrain, J.4
Main, D.5
Shields, P.G.6
-
32
-
-
0001146181
-
Family disclosure in genetic testing for cancer susceptibility: Determinants and consequences
-
Lerman, C., Peshkin, B. N., Hughes, C., & Issacs, C. (1998). Family disclosure in genetic testing for cancer susceptibility: Determinants and consequences. Journal of Health Care Law and Policy, 1, 353-372.
-
(1998)
Journal of Health Care Law and Policy
, vol.1
, pp. 353-372
-
-
Lerman, C.1
Peshkin, B.N.2
Hughes, C.3
Issacs, C.4
-
34
-
-
0035746393
-
Establishing priorities in neurofibromatosis research: A workshop summary
-
MacCollin, M., Gutmann, D. H., Korf, B., & Finkelstein, R. (2001). Establishing priorities in neurofibromatosis research: A workshop summary. Genetics in Medicine, 3(3), 212-217.
-
(2001)
Genetics in Medicine
, vol.3
, Issue.3
, pp. 212-217
-
-
MacCollin, M.1
Gutmann, D.H.2
Korf, B.3
Finkelstein, R.4
-
35
-
-
0034881346
-
Predictive genetic testing in children and adults: A study of emotional impact
-
Michie, S., Bobrow, S., Marteau, T. M., & the FAP Collaborative Research Group. (2001). Predictive genetic testing in children and adults: A study of emotional impact. Journal of Medical Genetics, 38, 519-526.
-
(2001)
Journal of Medical Genetics
, vol.38
, pp. 519-526
-
-
Michie, S.1
Bobrow, S.2
Marteau, T.M.3
-
36
-
-
0001846088
-
Predictive genetic testing in children: The need for psychological research
-
Michie, S., & Marteau, T. M. (1996). Predictive genetic testing in children: The need for psychological research. British Journal of Health Psychology, 1, 3-14.
-
(1996)
British Journal of Health Psychology
, vol.1
, pp. 3-14
-
-
Michie, S.1
Marteau, T.M.2
-
37
-
-
0030698638
-
At issue: Genes, experience, and chance in schizophrenia-positioning for the 21st century
-
Moldin, S. O., & Gottesman, I. I. (1997). At issue: Genes, experience, and chance in schizophrenia-positioning for the 21st century. Schizophrenia Bulletin, 23, 547-561.
-
(1997)
Schizophrenia Bulletin
, vol.23
, pp. 547-561
-
-
Moldin, S.O.1
Gottesman, I.I.2
-
38
-
-
0033978507
-
Genetic advances and learning disability
-
Muir, W. J. (2000). Genetic advances and learning disability. British Journal of Psychiatry, 176, 12-19.
-
(2000)
British Journal of Psychiatry
, vol.176
, pp. 12-19
-
-
Muir, W.J.1
-
39
-
-
0027566656
-
Epidemiology of colorectal adenomatous polyps
-
Neugut, A. I., Jacobson, J. S., & DeVivo, I. Epidemiology of colorectal adenomatous polyps. Cancer Epidemiology, Biomarkers, and Prevention, 2, 159-176.
-
Cancer Epidemiology, Biomarkers, and Prevention
, vol.2
, pp. 159-176
-
-
Neugut, A.I.1
Jacobson, J.S.2
DeVivo, I.3
-
41
-
-
0032764977
-
Psychiatric genetics: Progress, problems, and potential
-
Owen, M. J., & Cardno, A. G. (1999). Psychiatric genetics: Progress, problems, and potential. Lancet, 354(suppl 1), 11-14.
-
(1999)
Lancet
, vol.354
, Issue.SUPPL. 1
, pp. 11-14
-
-
Owen, M.J.1
Cardno, A.G.2
-
42
-
-
0030019446
-
Attitudes of 47 mothers of pediatric oncology patients
-
Patenaude, A. F., Basili, L., Fairclough, D., & Li, F. P. (1996). Attitudes of 47 mothers of pediatric oncology patients. Journal of Clinical Oncology, 14, 415-421.
-
(1996)
Journal of Clinical Oncology
, vol.14
, pp. 415-421
-
-
Patenaude, A.F.1
Basili, L.2
Fairclough, D.3
Li, F.P.4
-
43
-
-
0030466376
-
Genetic predisposition to organ-specific endpoints of alcoholism
-
Reed, T., Page, W. F., Viken, R. J., & Christian, J. C. (1996). Genetic predisposition to organ-specific endpoints of alcoholism. Alcoholism: Clinical and Experimental Research, 20, 1528-1533.
-
(1996)
Alcoholism: Clinical and Experimental Research
, vol.20
, pp. 1528-1533
-
-
Reed, T.1
Page, W.F.2
Viken, R.J.3
Christian, J.C.4
-
44
-
-
0024972478
-
False start on manic depression
-
Robertson, M. (1989). False start on manic depression. Nature, 342, 222.
-
(1989)
Nature
, vol.342
, pp. 222
-
-
Robertson, M.1
-
45
-
-
0032940422
-
Genetics and child psychiatry: I. Advances in quantitative and molecular genetics
-
Rutter, M., Silberg, J., O'Connor, T., & Simonoff, E. (1999a). Genetics and child psychiatry: I. Advances in quantitative and molecular genetics. Journal of Child Psychology and Psychiatry, 42, 3-18.
-
(1999)
Journal of Child Psychology and Psychiatry
, vol.42
, pp. 3-18
-
-
Rutter, M.1
Silberg, J.2
O'Connor, T.3
Simonoff, E.4
-
46
-
-
0032892309
-
Genetics and child psychiatry: II. Empirical research findings
-
Rutter, M., Silberg, J., O'Connor, T., & Simonoff, E. (1999b). Genetics and child psychiatry: II. Empirical research findings. Journal of Child Psychology and Psychiatry, 40, 19-55.
-
(1999)
Journal of Child Psychology and Psychiatry
, vol.40
, pp. 19-55
-
-
Rutter, M.1
Silberg, J.2
O'Connor, T.3
Simonoff, E.4
-
47
-
-
0032954046
-
Familial context of genetic testing for cancer susceptibility: Moderating effect of siblings' test results on psychological distress one to two weeks after BRCA1 mutation testing (1999)
-
Smith, K. R., West, J. A., Croyle, R. T., & Botkin, J. R. (1999). Familial context of genetic testing for cancer susceptibility: Moderating effect of siblings' test results on psychological distress one to two weeks after BRCA1 mutation testing (1999). Cancer Epidemiology, Biomarkers, and Prevention, 8, 385-392.
-
(1999)
Cancer Epidemiology, Biomarkers, and Prevention
, vol.8
, pp. 385-392
-
-
Smith, K.R.1
West, J.A.2
Croyle, R.T.3
Botkin, J.R.4
-
48
-
-
0035160552
-
Parental communication of BRCA1/2 genetic test results to children
-
Tercyak, K. P., Hughes, C., Main, D., Snyder, C., Lynch, J. F., Lynch, H. T., & Lerman, C. (2001). Parental communication of BRCA1/2 genetic test results to children. Patient Education and Counseling, 42, 213-224.
-
(2001)
Patient Education and Counseling
, vol.42
, pp. 213-224
-
-
Tercyak, K.P.1
Hughes, C.2
Main, D.3
Snyder, C.4
Lynch, J.F.5
Lynch, H.T.6
Lerman, C.7
-
49
-
-
0032936729
-
Predictive DNA testing for multiple endocrine neoplasia 2: A therapeutic challenge of prophylactic thryroidectomy in very young children
-
Van Heurn, L. W. E., Schaap, C., Sie, G., Haagen, A. A. M., Gerver, W. J., Freling, G., van Amstel, H. P., & Heineman, E. (1999). Predictive DNA testing for multiple endocrine neoplasia 2: A therapeutic challenge of prophylactic thryroidectomy in very young children. Journal of Pediatric Surgery, 34, 568-557.
-
(1999)
Journal of Pediatric Surgery
, vol.34
, pp. 568-557
-
-
Van Heurn, L.W.E.1
Schaap, C.2
Sie, G.3
Haagen, A.A.M.4
Gerver, W.J.5
Freling, G.6
Van Amstel, H.P.7
Heineman, E.8
-
50
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CHGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk, A. J., Pieretti, M., Sutcliffe, J. S., Fu, Y.-H., Kuhi, D. P., Pizzuti, A., Reiner, O., Richards, S., Victoria, M. F., Zhang, F., Eussen, B. E., Van Ommen, G. J., Blonden, L. A. Riggens, G. J., Chastain, J. L., Kunst, C. B., Galjaard, H., Caskey, C. T., Nelson, D. L., Oostra, B. A., & Warren, S. T. (1991). Identification of a gene (FMR-1) containing a CHGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell, 65, 905-914.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.-H.4
Kuhi, D.P.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.10
Eussen, B.E.11
Van Ommen, G.J.12
Blonden, L.A.13
Riggens, G.J.14
Chastain, J.L.15
Kunst, C.B.16
Galjaard, H.17
Caskey, C.T.18
Nelson, D.L.19
Oostra, B.A.20
Warren, S.T.21
more..
-
52
-
-
0028132846
-
Genetic testing for children and adolescents: Who decides?
-
Wertz, D. C., Fanos, J. H., & Reilly, P. R. (1994) Genetic testing for children and adolescents: Who decides? Journal of the American Medical Association, 272, 875-881.
-
(1994)
Journal of the American Medical Association
, vol.272
, pp. 875-881
-
-
Wertz, D.C.1
Fanos, J.H.2
Reilly, P.R.3
-
53
-
-
0009629810
-
Genetic epidemiology of soft soft tissue sarcomas in children
-
H. R. Mueller & W. Weber (Eds.). Basel: AG Karger
-
Williams, W. R., & Strong, L. C. (1985). Genetic epidemiology of soft soft tissue sarcomas in children. In H. R. Mueller & W. Weber (Eds.), Familial cancer: First International Research Conference. Basel: AG Karger.
-
(1985)
Familial Cancer: First International Research Conference
-
-
Williams, W.R.1
Strong, L.C.2
-
55
-
-
0021259895
-
A private view of heterozygosity: Eight-year follow-up study on carriers of the Tay-Sachs gene detected by high school screening in Montreal
-
Zeesman, S., Clow, C. L., Cartier, L., & Scriver, C. R. (1984). A private view of heterozygosity: Eight-year follow-up study on carriers of the Tay-Sachs gene detected by high school screening in Montreal. American Journal of Medical Genetics, 18, 769-778.
-
(1984)
American Journal of Medical Genetics
, vol.18
, pp. 769-778
-
-
Zeesman, S.1
Clow, C.L.2
Cartier, L.3
Scriver, C.R.4
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