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/vufind/Search/Results?lookfor=%22Fleming%2C+Jane%22&type=Person&sort=year
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PubPharm (111)
1
"We are not a typical family anymore" : Exploring the experiences and support needs of fathers of children with Fragile X syndrome in Australia
enthalten in:
American journal of medical genetics. Part A
| 2024
von
Luermans, J.
|
Fleming, J.
|
O'Shea, R.
| +3
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2
“We are not a typical family anymore” : Exploring the experiences and support needs of fathers of children with Fragile X syndrome in Australia
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2024
von
Luermans, J.
|
Fleming, J.
|
O'Shea, R.
| +3
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3
Variation in UK fracture liaison service consultation conduct and content before and during the COVID pandemic : results from the iFraP-D UK survey
enthalten in:
Archives of osteoporosis
| 2023
von
Bullock, L.
|
Abdelmagid, S.
|
Fleming, J.
| +8
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4
Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1
enthalten in:
Familial cancer
| 2023
von
Wilding, M.
|
Fleming, J.
|
Moore, K.
| +8
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5
Current and Emerging Imaging Techniques for Neurofibromatosis Type 1-Associated Cutaneous Neurofibromas
enthalten in:
The Journal of investigative dermatology
| 2023
von
Li, Y.
|
Blakeley, J.
|
Ly, I.
| +13
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6
Expanding the Australian Newborn Blood Spot Screening Program using genomic sequencing : do we want it and are we ready?
enthalten in:
European journal of human genetics : EJHG
| 2023
von
White, S.
|
Mossfield, T.
|
Fleming, J.
| +6
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7
Exploring the impact of the reclassification of a hereditary cancer syndrome gene variant : emerging themes from a qualitative study
enthalten in:
Journal of community genetics
| 2023
von
Wedd, L.
|
Gleeson, M.
|
Meiser, B.
| +11
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8
Exploring the impact of the reclassification of a hereditary cancer syndrome gene variant: emerging themes from a qualitative study
enthalten in:
Journal of community genetics
| 2023
von
Wedd, L.
|
Gleeson, M.
|
Meiser, B.
| +11
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9
Characterization of health concerns in people with neurofibromatosis type 1
enthalten in:
Molecular genetics & genomic medicine
| 2023
von
Fleming, J.
|
Morgan, O.
|
Wong, C.
| +2
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10
Characterization of health concerns in people with neurofibromatosis type 1
enthalten in:
Molecular Genetics & Genomic Medicine
| 2023
von
Fleming, J.
|
Morgan, O.
|
Wong, C.
| +2
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Medienart
111
Aufsätze
79
E-Artikel
79
E-Ressourcen
32
Gedruckte Aufsätze
Zeitschriftentitel
12
BMC geriatrics
5
Archives of osteoporosis
5
BMJ open
5
Human gene therapy
5
Journal of community genetics
4
Acta neuropathologica
4
Aging & mental health
4
Familial cancer
4
Journal of genetic counseling
3
BMC medical ethics
2
American Journal of Medical Genetics Part C: Se...
2
American journal of medical genetics. Part A
2
Australian and New Zealand journal of obstetric...
2
Emergency medicine journal
2
European journal of palliative care
2
International journal of epidemiology
2
Journal of Alzheimer's disease : JAD
2
Journal of Genetic Counseling
2
Neuro-oncology practice
2
Palliative medicine
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Thema
59
Journal Article
36
Research Support, Non-U.S. Gov't
9
Dementia
6
Review
6
dementia
5
Aged
5
Osteoporosis
5
iFraP
4
80 and over
4
ACT
4
ADRD
4
APOE
4
Biobank for aging studies
4
CC75C
4
CFAS
4
Consultation
4
Delphi survey
4
Epidemiology
4
Fracture Liaison Services
4
Genetic counseling
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Erscheinungszeitraum
106
2000-
1
1900-1999
Erscheinungsjahr(e)
Von:
Bis:
Sprache
90
Englisch
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