Early onset familial premature ovarian insufficiency - inclusion as a rare disease into genomics England 100 000 genome project

B. Cloke; E. Hoffmann; Z. Szallasi; T. Hillard; Edward Morris; N. Panay; Melanie Davies; G. Conway; P. Dixon; C. Williamson; J. Rymer

Early onset familial premature ovarian insufficiency - inclusion as a rare disease into genomics England 100 000 genome project

B. Cloke, E. Hoffmann, Z. Szallasi, T. Hillard, Edward Morris, N. Panay, Melanie Davies, G. Conway, P. Dixon, C. Williamson, J. Rymer

Original language	English
Publication date	Jun 2016
Publication status	Published - Jun 2016
Externally published	Yes
Event	RCOG World Congress 2016 - Birmingham, United Kingdom Duration: 20 Jun 2016 → 22 Jun 2016

Conference

Conference	RCOG World Congress 2016
Country/Territory	United Kingdom
City	Birmingham
Period	20/06/2016 → 22/06/2016

Cite this

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title = "Early onset familial premature ovarian insufficiency - inclusion as a rare disease into genomics England 100 000 genome project",

author = "B. Cloke and E. Hoffmann and Z. Szallasi and T. Hillard and Edward Morris and N. Panay and Melanie Davies and G. Conway and P. Dixon and C. Williamson and J. Rymer",

year = "2016",

month = jun,

language = "English",

note = "RCOG World Congress 2016 ; Conference date: 20-06-2016 Through 22-06-2016",

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TY - CONF

T1 - Early onset familial premature ovarian insufficiency - inclusion as a rare disease into genomics England 100 000 genome project

AU - Cloke, B.

AU - Hoffmann, E.

AU - Szallasi, Z.

AU - Hillard, T.

AU - Morris, Edward

AU - Panay, N.

AU - Davies, Melanie

AU - Conway, G.

AU - Dixon, P.

AU - Williamson, C.

AU - Rymer, J.

PY - 2016/6

Y1 - 2016/6

M3 - Poster

T2 - RCOG World Congress 2016

Y2 - 20 June 2016 through 22 June 2016

ER -