-
1
-
-
70549110830
-
A sociolinguistic exploration of genetic counseling discourse involving a child with a new genetic diagnosis
-
Babul-Hirji R, Hewson S, Frescura M. 2010. A sociolinguistic exploration of genetic counseling discourse involving a child with a new genetic diagnosis. Patient Educ Couns 78:40-45.
-
(2010)
Patient Educ Couns
, vol.78
, pp. 40-45
-
-
Babul-Hirji, R.1
Hewson, S.2
Frescura, M.3
-
2
-
-
1842483083
-
Parents of children with intellectual disabilities: Their expectations and experience of genetic counselling
-
Barr O, Millar R. 2003. Parents of children with intellectual disabilities: Their expectations and experience of genetic counselling. J Appl Res Intellect Disabil 16:189-204.
-
(2003)
J Appl Res Intellect Disabil
, vol.16
, pp. 189-204
-
-
Barr, O.1
Millar, R.2
-
3
-
-
46249119469
-
A different type of appointment: The experiences of parents who have children with intellectual disabilities referred for genetic investigation
-
Barr O, McConkey R. 2007. A different type of appointment: The experiences of parents who have children with intellectual disabilities referred for genetic investigation. J Res Nurs 12:637-652.
-
(2007)
J Res Nurs
, vol.12
, pp. 637-652
-
-
Barr, O.1
McConkey, R.2
-
4
-
-
0035260861
-
A process for delivering bad news: Supporting families when a child is diagnosed
-
Boyd JR. 2001. A process for delivering bad news: Supporting families when a child is diagnosed. J Neurosci Nurs 33:14-20.
-
(2001)
J Neurosci Nurs
, vol.33
, pp. 14-20
-
-
Boyd, J.R.1
-
6
-
-
0030833282
-
Clinical Terminology: Anxiety and confusion amongst families undergoing genetic counseling
-
Chapple A, Campion P, May C. 2006. Clinical Terminology: Anxiety and confusion amongst families undergoing genetic counseling. Patient Educ Couns 32:81-91.
-
(2006)
Patient Educ Couns
, vol.32
, pp. 81-91
-
-
Chapple, A.1
Campion, P.2
May, C.3
-
8
-
-
0037243129
-
Parents' stories of sensitive and insensitive care by paediatricians in the time leading up to and including diagnostic disclosure of a life-limiting condition in their child
-
Davies R, Davis B, Sibert J. 2003. Parents' stories of sensitive and insensitive care by paediatricians in the time leading up to and including diagnostic disclosure of a life-limiting condition in their child. Child Care Health Dev 29:77-83.
-
(2003)
Child Care Health Dev
, vol.29
, pp. 77-83
-
-
Davies, R.1
Davis, B.2
Sibert, J.3
-
9
-
-
33748051094
-
Breaking difficult news in a newborn setting: Down syndrome as a paradigm
-
Dent KM, Carey JC. 2006. Breaking difficult news in a newborn setting: Down syndrome as a paradigm. Am J Med Genet Part C 142C:173-179.
-
(2006)
Am J Med Genet Part C
, vol.142 C
, pp. 173-179
-
-
Dent, K.M.1
Carey, J.C.2
-
11
-
-
34247149788
-
Why do we need a diagnosis A qualitative study of parents experiences, coping and needs when the newborn child is severely disabled
-
Graungaard AH, Skov L. 2007. Why do we need a diagnosis A qualitative study of parents experiences, coping and needs when the newborn child is severely disabled. Child Care Health Dev 33:296-307.
-
(2007)
Child Care Health Dev
, vol.33
, pp. 296-307
-
-
Graungaard, A.H.1
Skov, L.2
-
12
-
-
77954077625
-
What do we know about giving bad news? A Review
-
Harrison ME, Walling A. 2010. What do we know about giving bad news? A Review. Clin Pediatr 49:619-626.
-
(2010)
Clin Pediatr
, vol.49
, pp. 619-626
-
-
Harrison, M.E.1
Walling, A.2
-
13
-
-
33751018539
-
Uncertainty and perceived personal control among parents of children with rare chromosome conditions: The role of genetic counseling
-
Lipinski SE, Lipinski MJ, Biesecker LG, Biesecker BB. 1997. Uncertainty and perceived personal control among parents of children with rare chromosome conditions: The role of genetic counseling. Am J Med Genet Part C 142C:232-240.
-
(1997)
Am J Med Genet Part C
, vol.142 C
, pp. 232-240
-
-
Lipinski, S.E.1
Lipinski, M.J.2
Biesecker, L.G.3
Biesecker, B.B.4
-
14
-
-
70449397325
-
Parental perceived value of a diagnosis for intellectual disability (ID): A qualitative comparison of families with and without a diagnosis for their child's ID
-
Makela NL, Birch PH, Friedman JM, Marra CA. 2009. Parental perceived value of a diagnosis for intellectual disability (ID): A qualitative comparison of families with and without a diagnosis for their child's ID. Am J Med Genet Part A 149A:2393-2402.
-
(2009)
Am J Med Genet Part A
, vol.149 A
, pp. 2393-2402
-
-
Makela, N.L.1
Birch, P.H.2
Friedman, J.M.3
Marra, C.A.4
-
15
-
-
53949100046
-
Assessment of the content and process of genetic counseling: A critical review of empirical studies
-
Meiser B, Irle J, Lobb E, Barlow-Stewart K. 2008. Assessment of the content and process of genetic counseling: A critical review of empirical studies. J Genet Couns 17:434-451.
-
(2008)
J Genet Couns
, vol.17
, pp. 434-451
-
-
Meiser, B.1
Irle, J.2
Lobb, E.3
Barlow-Stewart, K.4
-
16
-
-
38049161815
-
Breaking bad news: A practical approach for the hospitalist
-
Minichiello TA, Ling D, Ucci DK. 2007. Breaking bad news: A practical approach for the hospitalist. J Hosp Med 2:415-421.
-
(2007)
J Hosp Med
, vol.2
, pp. 415-421
-
-
Minichiello, T.A.1
Ling, D.2
Ucci, D.K.3
-
17
-
-
0032057022
-
Practical strategies for combining qualitative and quantitative methods: Applications to health research
-
Morgan DL. 1998. Practical strategies for combining qualitative and quantitative methods: Applications to health research. Qual Health Res 8:362-376.
-
(1998)
Qual Health Res
, vol.8
, pp. 362-376
-
-
Morgan, D.L.1
-
18
-
-
44849139821
-
Expanding newborn screening: Process, policy, and priorities. United States Preventive Services Task Force
-
Moyer VA, Calonge N, Teutsch SM, Botkin JR. 2008. Expanding newborn screening: Process, policy, and priorities. United States Preventive Services Task Force. Hastings Cent Rep 38:32-39.
-
(2008)
Hastings Cent Rep
, vol.38
, pp. 32-39
-
-
Moyer, V.A.1
Calonge, N.2
Teutsch, S.M.3
Botkin, J.R.4
-
19
-
-
84856718448
-
What does it mean?": Uncertainties in understanding results of chromosomal microarray testing
-
Reiff M, Bernhardt BA, Mulchandani S, Soucier D, Cornell D, Pyeritz RE, Spinner NB. 2012. " What does it mean?": Uncertainties in understanding results of chromosomal microarray testing. Genet Med 14:250-258.
-
(2012)
Genet Med
, vol.14
, pp. 250-258
-
-
Reiff, M.1
Bernhardt, B.A.2
Mulchandani, S.3
Soucier, D.4
Cornell, D.5
Pyeritz, R.E.6
Spinner, N.B.7
-
20
-
-
85174220939
-
-
In: Coleman WB, Tsongalis GJ, editors. Molecular diagnostics: For the clinical laboratorian, 2nd edition. Totowa, New Jersey: Humana Press, a part of Springer Science+Business Media, LLC.
-
Roche M. 2006. Genetic counseling considerations in molecular diagnosis. In: Coleman WB, Tsongalis GJ, editors. Molecular diagnostics: For the clinical laboratorian, 2nd edition. Totowa, New Jersey: Humana Press, a part of Springer Science+Business Media, LLC. pp 525-544.
-
(2006)
Genetic counseling considerations in molecular diagnosis
, pp. 525-544
-
-
Roche, M.1
-
21
-
-
37349011966
-
Breaking bad news
-
Schoefl R. 2008. Breaking bad news. Dig Dis 26:56-58.
-
(2008)
Dig Dis
, vol.26
, pp. 56-58
-
-
Schoefl, R.1
-
22
-
-
33746586482
-
Parental experience of a pediatric genetic referral
-
Skirton H. 2006. Parental experience of a pediatric genetic referral. Am J Matern Child Nurs 31:178-184.
-
(2006)
Am J Matern Child Nurs
, vol.31
, pp. 178-184
-
-
Skirton, H.1
-
23
-
-
14644404232
-
Mothers of children with Down syndrome reflect on their postnatal support
-
Skotko B. 2005. Mothers of children with Down syndrome reflect on their postnatal support. Pediatrics 115:64-77.
-
(2005)
Pediatrics
, vol.115
, pp. 64-77
-
-
Skotko, B.1
-
24
-
-
70349747042
-
Postnatal diagnosis of Down syndrome: Synthesis of the evidence on how best to deliver the news
-
for the Down Syndrome Diagnosis Study Group.
-
Skotko BG, Capone GT, Kishnani PS. for the Down Syndrome Diagnosis Study Group. 2009. Postnatal diagnosis of Down syndrome: Synthesis of the evidence on how best to deliver the news. Pediatrics 124:e751-e758.
-
(2009)
Pediatrics
, vol.124
-
-
Skotko, B.G.1
Capone, G.T.2
Kishnani, P.S.3
-
26
-
-
84874203601
-
Hearing from parents: The impact of receiving the diagnosis of Williams syndrome in their child
-
Waxler JL, Cherniske EM, Dieter K, Herd P, Pober BR. 2013. Hearing from parents: The impact of receiving the diagnosis of Williams syndrome in their child. Am J Med Genet Part A 161:534-541.
-
(2013)
Am J Med Genet Part A
, vol.161
, pp. 534-541
-
-
Waxler, J.L.1
Cherniske, E.M.2
Dieter, K.3
Herd, P.4
Pober, B.R.5
|