Improving rare disease identification and coordinating health and social care priorities

Original language	English
Article number	P19.39C
Journal	European Journal of Human Genetics
Volume	27
Publication status	Published - 03 Jul 2019

Student theses

• Improving communication and identifying priorities for modernising rare disease services with healthcare practitioners, patients, families and advocacy groups

  Crowe, A. L. (Author), McKnight, A. (Supervisor) & Duffy, G. (Supervisor), Dec 2023

  Student thesis: Doctoral Thesis › Doctor of Philosophy

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McAneney, H., Crowe, A., Millar, J., Kerr, K., McMullan, J., & McKnight, A. J. (2019). Improving rare disease identification and coordinating health and social care priorities. European Journal of Human Genetics, 27, Article P19.39C.

McAneney, H. ; Crowe, A. ; Millar, J. et al. / Improving rare disease identification and coordinating health and social care priorities. In: European Journal of Human Genetics. 2019 ; Vol. 27.

@article{4a8aabf438e740a4a9624acb0a5e4334,

title = "Improving rare disease identification and coordinating health and social care priorities",

author = "H. McAneney and A. Crowe and J. Millar and K. Kerr and J. McMullan and McKnight, {A. J.}",

year = "2019",

month = jul,

day = "3",

language = "English",

volume = "27",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

}

McAneney, H, Crowe, A, Millar, J, Kerr, K, McMullan, J & McKnight, AJ 2019, 'Improving rare disease identification and coordinating health and social care priorities', European Journal of Human Genetics, vol. 27, P19.39C.

Improving rare disease identification and coordinating health and social care priorities. / McAneney, H.; Crowe, A.; Millar, J. et al.
In: European Journal of Human Genetics, Vol. 27, P19.39C, 03.07.2019.

Research output: Contribution to journal › Meeting abstract › peer-review

TY - JOUR

T1 - Improving rare disease identification and coordinating health and social care priorities

AU - McAneney, H.

AU - Crowe, A.

AU - Millar, J.

AU - Kerr, K.

AU - McMullan, J.

AU - McKnight, A. J.

PY - 2019/7/3

Y1 - 2019/7/3

M3 - Meeting abstract

SN - 1018-4813

VL - 27

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

M1 - P19.39C

ER -

McAneney H, Crowe A, Millar J, Kerr K, McMullan J, McKnight AJ. Improving rare disease identification and coordinating health and social care priorities. European Journal of Human Genetics. 2019 Jul 3;27:P19.39C.