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Germline FH mutations presenting with pheochromocytoma.
Published in:
2014
By:
- Clark, Graeme R;
- Sciacovelli, Marco;
- Gaude, Edoardo;
- Walsh, Diana M;
- Kirby, Gail;
- Simpson, Michael A;
- Trembath, Richard C;
- Berg, Jonathan N;
- Woodward, Emma R;
- Kinning, Esther;
- Morrison, Patrick J;
- Frezza, Christian;
- Maher, Eamonn R
Publication type:
journal article
Social Media and Active Shooter Events: A School Crisis Communication Challenge.
Published in:
Qualitative Research Reports in Communication, 2017, v. 18, n. 1, p. 8, doi. 10.1080/17459435.2016.1247111
By:
- Thompson, Blair;
- Mazer, Joseph P.;
- Payne, Holly J.;
- Jerome, Angela M.;
- Kirby, E. Gail;
- Pfohl, William
Publication type:
Article
Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies.
Published in:
2009
By:
- Lim, Derek;
- Bowdin, Sarah C;
- Tee, Louise;
- Kirby, Gail A;
- Blair, Edward;
- Fryer, Alan;
- Lam, Wayne;
- Oley, Christine;
- Cole, Trevor;
- Brueton, Louise A;
- Reik, Wolf;
- Macdonald, Fiona;
- Maher, Eamonn R
Publication type:
journal article
Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies.
Published in:
Human Reproduction, 2009, v. 24, n. 3, p. 741
By:
- Derek Lim;
- Sarah C. Bowdin;
- Louise Tee;
- Gail A. Kirby;
- Edward Blair;
- Alan Fryer;
- Wayne Lam;
- Christine Oley;
- Trevor Cole;
- Louise A. Brueton;
- Wolf Reik;
- Fiona Macdonald;
- Eamonn R. Maher
Publication type:
Article
A survey of assisted reproductive technology births and imprinting disorders.
Published in:
Human Reproduction, 2007, v. 22, n. 12, p. 3237, doi. 10.1093/humrep/dem268
By:
- Sarah Bowdin;
- Cathy Allen;
- Gail Kirby;
- Louise Brueton;
- Masoud Afnan;
- Christopher Barratt;
- Jackson Kirkman-Brown;
- Robert Harrison;
- Eamonn R Maher;
- William Reardon
Publication type:
Article
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD.
Published in:
Human Mutation, 2010, v. 31, n. 1, p. 41, doi. 10.1002/humu.21136
By:
- Ricketts, Christopher J.;
- Forman, Julia R.;
- Rattenberry, Eleanor;
- Bradshaw, Nicola;
- Lalloo, Fiona;
- Izatt, Louise;
- Cole, Trevor R.;
- Armstrong, Ruth;
- Kumar, V.K. Ajith;
- Morrison, Patrick J.;
- Atkinson, A. Brew;
- Douglas, Fiona;
- Ball, Steve G.;
- Cook, Jackie;
- Srirangalingam, Umasuthan;
- Killick, Pip;
- Kirby, Gail;
- Aylwin, Simon;
- Woodward, Emma R.;
- Evans, D. Gareth R.
Publication type:
Article
Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism.
Published in:
Clinical Endocrinology, 2010, v. 73, n. 5, p. 671, doi. 10.1111/j.1365-2265.2010.03849.x
By:
- Cangul, Hakan;
- Morgan, Neil V.;
- Forman, Julia R.;
- Saglam, Halil;
- Aycan, Zehra;
- Yakut, Tahsin;
- Gulten, Tuna;
- Tarim, Omer;
- Bober, Ece;
- Cesur, Yasar;
- Kirby, Gail A.;
- Pasha, Shanaz;
- Karkucak, Mutlu;
- Eren, Erdal;
- Cetinkaya, Semra;
- Bas, Veysel;
- Demir, Korcan;
- Yuca, Sevil A.;
- Meyer, Esther;
- Kendall, Michaela
Publication type:
Article

Found: 7

Germline FH mutations presenting with pheochromocytoma.

Social Media and Active Shooter Events: A School Crisis Communication Challenge.

Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies.

Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies.

A survey of assisted reproductive technology births and imprinting disorders.

Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD.

Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism.