Detalles de la búsqueda
1.
Clinical audit of genetic testing and referral patterns for fragile X and associated conditions.
Am J Med Genet A
; 170(6): 1439-49, 2016 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-26892444
2.
Embodied experiences of prenatal diagnosis of fetal abnormality and pregnancy termination.
Reprod Health Matters
; 24(47): 168-77, 2016 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-27578350
3.
'A short time but a lovely little short time': Bereaved parents' experiences of having a child with spinal muscular atrophy type 1.
J Paediatr Child Health
; 52(1): 40-6, 2016 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-26437687
4.
Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research.
Genet Med
; 16(3): 207-16, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24030436
5.
Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention.
BMC Med Genet
; 15: 33, 2014 Mar 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-24628824
6.
Cascade carrier testing after a child is diagnosed with cystic fibrosis through newborn screening: investigating why most relatives do not have testing.
Genet Med
; 15(7): 533-40, 2013 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-23348769
7.
Development and use of the Australian reproductive genetic carrier screening decision aid.
Eur J Hum Genet
; 30(2): 194-202, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34725472
8.
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation.
J Pers Med
; 12(11)2022 Oct 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-36579509
9.
Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education.
Front Genet
; 11: 59, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32194615
10.
Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning.
Front Genet
; 11: 151, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32194628
11.
'It is not in my world': an exploration of attitudes and influences associated with cystic fibrosis carrier screening.
Eur J Hum Genet
; 16(4): 435-44, 2008 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-18059419
12.
Parental experiences after prenatal diagnosis of fetal abnormality.
Semin Fetal Neonatal Med
; 23(2): 150-154, 2018 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-29258838
13.
A case for cystic fibrosis carrier testing in the general population.
Med J Aust
; 194(4): 208-9, 2011 Feb 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-21401469
14.
A mixed methods exploration of families' experiences of the diagnosis of childhood spinal muscular atrophy.
Eur J Hum Genet
; 23(5): 575-80, 2015 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-25074464
15.
A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy.
Eur J Hum Genet
; 23(10): 1294-300, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-25626706
16.
How do women at increased, but unexplained, familial risk of breast cancer perceive and manage their risk? A qualitative interview study.
Hered Cancer Clin Pract
; 9(1): 7, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-21896163
17.
Uptake of carrier testing in families after cystic fibrosis diagnosis through newborn screening.
Eur J Hum Genet
; 18(10): 1084-9, 2010 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-20512163
18.
Perceived relevance of genetic carrier screening: observations of the role of health-related life experiences and stage of life in decision making.
J Community Genet
; 3(1): 47-54, 2012 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-22109909
Resultados
1 -
18
de 18
1
Próxima >
>>