-
1
-
-
0028872836
-
Points to consider: Ethical, legal, and psychosocial implications of genetic testing in children and adolescents
-
American Society of Human Genetics and American College of Medical Genetics. 1995. Points to consider: Ethical, legal, and psychosocial implications of genetic testing in children and adolescents. Am J Hum Genet 57:1233-1241.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1233-1241
-
-
-
2
-
-
0141706635
-
Standards for the diagnosis and management of individuals with alpha-1 antitrypsin deficiency
-
American Thoracic Society/European Respiratory Society Statement. 2003. Standards for the diagnosis and management of individuals with alpha-1 antitrypsin deficiency. Am J Respir Crit Care Med 168:818-900.
-
(2003)
Am J Respir Crit Care Med
, vol.168
, pp. 818-900
-
-
-
3
-
-
0037468422
-
A survey of liver transplantation from living adult donors in the United States
-
Brown RS, Russo MW, Lai M, Shiffman ML, Richardson MC, Everhart JE, Hoofnagle JH. 2003. A survey of liver transplantation from living adult donors in the United States. N Engl J Med 348:818-825.
-
(2003)
N Engl J Med
, vol.348
, pp. 818-825
-
-
Brown, R.S.1
Russo, M.W.2
Lai, M.3
Shiffman, M.L.4
Richardson, M.C.5
Everhart, J.E.6
Hoofnagle, J.H.7
-
4
-
-
0036433482
-
Worldwide racial and ethnic distribution of alpha 1-antitrypsin deficiency: Summary of an analysis of published genetic epidemiologic surveys
-
de Serres FJ. 2002. Worldwide racial and ethnic distribution of alpha 1-antitrypsin deficiency: Summary of an analysis of published genetic epidemiologic surveys. Chest 122:1818-1829.
-
(2002)
Chest
, vol.122
, pp. 1818-1829
-
-
De Serres, F.J.1
-
7
-
-
0032822883
-
The missing link in linkage analysis: The well sibling revisited
-
Fanos JH. 1999a. The missing link in linkage analysis: The well sibling revisited. Genet Test 3:273-278.
-
(1999)
Genet Test
, vol.3
, pp. 273-278
-
-
Fanos, J.H.1
-
8
-
-
0033407102
-
My crooked vision: The well sib views ataxia-telangiectasia
-
Fanos JH. 1999b. My crooked vision: The well sib views ataxia-telangiectasia. Am J Med Genet 87:420-425.
-
(1999)
Am J Med Genet
, vol.87
, pp. 420-425
-
-
Fanos, J.H.1
-
9
-
-
0032871643
-
A mark on the arm: Myths of carrier status in sibs of individuals with ataxia-telangiectasia
-
Fanos JH, Gatti RA. 1999. A mark on the arm: Myths of carrier status in sibs of individuals with ataxia-telangiectasia. Am J Med Genet 86:338-346.
-
(1999)
Am J Med Genet
, vol.86
, pp. 338-346
-
-
Fanos, J.H.1
Gatti, R.A.2
-
10
-
-
0029011920
-
Perception of carrier status by cystic fibrosis siblings
-
Fanos JH, Johnson JP. 1995a. Perception of carrier status by cystic fibrosis siblings. Am J Hum Genet 57:431-438.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 431-438
-
-
Fanos, J.H.1
Johnson, J.P.2
-
11
-
-
0029091299
-
Barriers to carrier testing for adult cystic fibrosis sibs: The importance of not knowing
-
Fanos JH, Johnson JP. 1995b. Barriers to carrier testing for adult cystic fibrosis sibs: The importance of not knowing. Am J Med Genet 59:85-91.
-
(1995)
Am J Med Genet
, vol.59
, pp. 85-91
-
-
Fanos, J.H.1
Johnson, J.P.2
-
12
-
-
0033452444
-
Never again joy without sorrow: The effect on parents of a child with ataxia-telangiectasia
-
Fanos JH, Mackintosh MA. 1999. Never again joy without sorrow: The effect on parents of a child with ataxia-telangiectasia. Am J Med Genet 87:413-419.
-
(1999)
Am J Med Genet
, vol.87
, pp. 413-419
-
-
Fanos, J.H.1
Mackintosh, M.A.2
-
13
-
-
0035157769
-
Family pictures: The impact of growing up with a brother with X-linked severe combined immunodeficiency
-
Fanos JH, Puck JM. 2001. Family pictures: The impact of growing up with a brother with X-linked severe combined immunodeficiency. Am J Med Genet 98:57-63.
-
(2001)
Am J Med Genet
, vol.98
, pp. 57-63
-
-
Fanos, J.H.1
Puck, J.M.2
-
14
-
-
0035149760
-
Sib understanding of genetics and attitudes toward carrier testing for X-linked severe combined immunodeficiency
-
Fanos JH, Davis J, Puck JM. 2001. Sib understanding of genetics and attitudes toward carrier testing for X-linked severe combined immunodeficiency. Am J Med Genet 98:46-56.
-
(2001)
Am J Med Genet
, vol.98
, pp. 46-56
-
-
Fanos, J.H.1
Davis, J.2
Puck, J.M.3
-
15
-
-
0024573753
-
Predictive testing for Huntington disease: I. Description of a pilot project in British Columbia
-
Fox S, Bloch M, Fahy M, Hayden MR. 1989. Predictive testing for Huntington disease: I. Description of a pilot project in British Columbia. Am J Med Genet 32:211-216.
-
(1989)
Am J Med Genet
, vol.32
, pp. 211-216
-
-
Fox, S.1
Bloch, M.2
Fahy, M.3
Hayden, M.R.4
-
16
-
-
0029440688
-
Testing children for genetic predispositions: Is it in their interest?
-
Hoffmann DE, Wulfsberg E. 1995. Testing children for genetic predispositions: Is it in their interest? J Law Med Ethics 23:331-344.
-
(1995)
J Law Med Ethics
, vol.23
, pp. 331-344
-
-
Hoffmann, D.E.1
Wulfsberg, E.2
-
17
-
-
0023685024
-
Invited essay on the psychological aspects of genetic counseling. V. Preselection: A family coping strategy in Huntington Disease
-
Kessler S. 1988. Invited essay on the psychological aspects of genetic counseling. V. Preselection: A family coping strategy in Huntington Disease. Am J Med Genet 31:617-621.
-
(1988)
Am J Med Genet
, vol.31
, pp. 617-621
-
-
Kessler, S.1
-
18
-
-
0020586516
-
Assignment of the alpha 1-antitrypsin gene and a sequence-related gene to human chromosome 14 by molecular hybridization
-
Lai EC, Kao FT, Law ML, Woo SL. 1983. Assignment of the alpha 1-antitrypsin gene and a sequence-related gene to human chromosome 14 by molecular hybridization. Am J Hum Genet 35:385-392.
-
(1983)
Am J Hum Genet
, vol.35
, pp. 385-392
-
-
Lai, E.C.1
Kao, F.T.2
Law, M.L.3
Woo, S.L.4
-
19
-
-
0027280593
-
Mammography adherences and psychological distress among women at risk for breast cancer
-
Lerman C, Daly M, Sands C, Balshem A, Lustbader E, Heggan T, Goldstein L, James J, Engstrom P. 1993. Mammography adherences and psychological distress among women at risk for breast cancer. J Natl Cancer Inst 85:1074-1080.
-
(1993)
J Natl Cancer Inst
, vol.85
, pp. 1074-1080
-
-
Lerman, C.1
Daly, M.2
Sands, C.3
Balshem, A.4
Lustbader, E.5
Heggan, T.6
Goldstein, L.7
James, J.8
Engstrom, P.9
-
21
-
-
0021752456
-
Complete sequence of the cDNA for human alpha 1-antitrypsin and the gene for the S variant
-
Long GL, Chandra T, Woo SL, Davie EW, Kurachi K. 1984. Complete sequence of the cDNA for human alpha 1-antitrypsin and the gene for the S variant. Biochemistry 23:4828-4837.
-
(1984)
Biochemistry
, vol.23
, pp. 4828-4837
-
-
Long, G.L.1
Chandra, T.2
Woo, S.L.3
Davie, E.W.4
Kurachi, K.5
-
22
-
-
0038624107
-
Ethical issues with genetic testing in pediatrics
-
Nelson RM, Botkin JR, Kodish ED, Levetown M, Truman JT, Wilfond BS, Harrrison CE, Kazura A, Krug E, Schwartz PA, Donovan GK, Fallat M, Porter IH, Steinberg D, Committee on Bioethics. 2001. Ethical issues with genetic testing in pediatrics. Pediatrics 107:1451-1455.
-
(2001)
Pediatrics
, vol.107
, pp. 1451-1455
-
-
Nelson, R.M.1
Botkin, J.R.2
Kodish, E.D.3
Levetown, M.4
Truman, J.T.5
Wilfond, B.S.6
Harrrison, C.E.7
Kazura, A.8
Krug, E.9
Schwartz, P.A.10
Donovan, G.K.11
Fallat, M.12
Porter, I.H.13
Steinberg, D.14
-
24
-
-
0031292156
-
Cystic fibrosis carrier population screening: A review
-
Rowley PT, Loader S, Levenkron JC. 1997. Cystic fibrosis carrier population screening: A review. Genet Test 1:53-59.
-
(1997)
Genet Test
, vol.1
, pp. 53-59
-
-
Rowley, P.T.1
Loader, S.2
Levenkron, J.C.3
-
25
-
-
0035135566
-
Susceptibility genes for rapid decline of lung function in the lung health study
-
Sandford AJ, Chagani T, Weir TD, Connett JE, Anthonisen NR, Pare PD. 2001. Susceptibility genes for rapid decline of lung function in the lung health study. Am J Respir Crit Care Med 163:469-473.
-
(2001)
Am J Respir Crit Care Med
, vol.163
, pp. 469-473
-
-
Sandford, A.J.1
Chagani, T.2
Weir, T.D.3
Connett, J.E.4
Anthonisen, N.R.5
Pare, P.D.6
-
26
-
-
0024434432
-
Alpha-1-antitrypsin deficiency. High prevalence in the St. Louis area determined by direct population screening
-
Silverman EK, Miletich JP, Pierce JA, Sherman LA, Endicott SK, Broze GJ, Jr., Campbell EJ. 1989. Alpha-1-antitrypsin deficiency. High prevalence in the St. Louis area determined by direct population screening. Am Rev Respir Dis 140:961-966.
-
(1989)
Am Rev Respir Dis
, vol.140
, pp. 961-966
-
-
Silverman, E.K.1
Miletich, J.P.2
Pierce, J.A.3
Sherman, L.A.4
Endicott, S.K.5
Broze Jr., G.J.6
Campbell, E.J.7
-
27
-
-
0006420960
-
Carrier testing among CF patients' first and second degree relatives
-
Sorenson JR, DeVellis BM, Cheuvront JB, Callanan NP, Talton SL. 1994. Carrier testing among CF patients' first and second degree relatives. Am J Hum Genet 555:A22.
-
(1994)
Am J Hum Genet
, vol.555
-
-
Sorenson, J.R.1
DeVellis, B.M.2
Cheuvront, J.B.3
Callanan, N.P.4
Talton, S.L.5
-
28
-
-
0028342899
-
Cystic fibrosis carrier screening in a high-risk population: Participation based on a traditional recruitment process
-
Surh LC, Cappelli M, MacDonald NE, Mettler G, Dales RE. 1994. Cystic fibrosis carrier screening in a high-risk population: Participation based on a traditional recruitment process. Arch Pediatr Adolesc Med 148: 632-637.
-
(1994)
Arch Pediatr Adolesc Med
, vol.148
, pp. 632-637
-
-
Surh, L.C.1
Cappelli, M.2
MacDonald, N.E.3
Mettler, G.4
Dales, R.E.5
-
29
-
-
0033362082
-
Transmitting genetic risk information in families: Attitudes about disclosing the identity of relatives
-
Wilcke JTR, Seersholm N, Kok-Jensen A, Dirksen A. 1999. Transmitting genetic risk information in families: Attitudes about disclosing the identity of relatives. Am J Hum Genet 65:902-909.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 902-909
-
-
Wilcke, J.T.R.1
Seersholm, N.2
Kok-Jensen, A.3
Dirksen, A.4
-
30
-
-
2642680855
-
1-antitrypsin deficiency: Memorandum from a WHO meeting
-
1-antitrypsin deficiency: Memorandum from a WHO meeting. Bull World Health Organ 75: 397-415.
-
(1997)
Bull World Health Organ
, vol.75
, pp. 397-415
-
-
|