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1

Is a theology for the poor relevant in a British society supported by benefits and a free NHS?

Homfray-Cooper, Trevor

Journal:

Journal of the European Pentecostal Theological Association

Year:

2018

Language:

english

File:

PDF, 1.58 MB

english, 2018

2

Existentialism, Eschatology and Wisdom: Canon Law as an Interim Agent of the Kingdom

Homfray, Kenyon

Journal:

Ecclesiastical Law Journal

Year:

2007

Language:

english

File:

PDF, 237 KB

english, 2007

3

Sir Edward Coke Gets It Wrong? A Brief History of Consecration

Homfray, Kenyon

Journal:

Ecclesiastical Law Journal

Year:

2009

Language:

english

File:

PDF, 240 KB

english, 2009

4

Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteria

N. E. Beck, I. P. M. Tomlinson, Tessa Homfray, I. Frayling, Shirley V. Hodgson, Chris Harocopos, Walter F. Bodmer

Journal:

Year:

1997

Language:

english

File:

PDF, 63 KB

english, 1997

5

Cerebral organoids model human brain development and microcephaly

Lancaster, Madeline A., Renner, Magdalena, Martin, Carol-Anne, Wenzel, Daniel, Bicknell, Louise S., Hurles, Matthew E., Homfray, Tessa, Penninger, Josef M., Jackson, Andrew P., Knoblich, Juergen A.

Journal:

Year:

2013

Language:

english

File:

PDF, 4.57 MB

english, 2013

6

Twining's Textbook of Fetal Abnormalities || Fetal Anomalies – The Geneticist's Approach

Year:

2015

Language:

english

File:

PDF, 1.56 MB

english, 2015

7

Standpoint, Objectivity, and Social Construction: Reflections from the Study of Gay and Lesbian Communities

Journal:

Sociological Research Online

Year:

2008

Language:

english

File:

PDF, 154 KB

english, 2008

8

Reproductive Genetics || Ethical aspects of saviour siblings: procreative reasons and the treatment of children

Kehoe, Sean, Chitty, Lyn, Homfray, Tessa

Year:

2009

Language:

english

File:

PDF, 149 KB

english, 2009

9

Defects in mismatch repair occur after APC mutations in the pathogenesis of sporadic colorectal tumours

TFR Homfray, SE Cottrell, M Ilyas, A Rowan, IC Talbot, WF Bodmer, IPM Tomlinson

Journal:

Year:

1998

Language:

english

File:

PDF, 213 KB

english, 1998

10

Clinical and hematologic aspects of the X-linked α-thalassemia/mental retardation syndrome (ATR-X)

R. J. Gibbons, L. Brueton, V. J. Buckle, J. Burn, J. Clayton-Smith, B. C. C. Davison, R. J. M. Gardner, T. Homfray, L. Kearney, H. M. Kingston, R. Newbury-Ecob, M. E. P. Porteous, A. O. M. Wilkie, Dr.

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 1.13 MB

english, 1995

11

A newly recognized autosomal recessive syndrome with abnormal vertebral ossification, rib abnormalities, and nephrogenic rests

Federico Prefumo, Tessa Homfray, Iona Jeffrey, Isabella Moore, Baskaran Thilaganathan

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 61 KB

english, 2003

12

Congenital vascular malformations: A series of five prenatally diagnosed cases

Fiona Connell, Tessa Homfray, Baskaran Thilaganathan, Amarnath Bhide, Iona Jeffrey, Renata Hutt, Peter Mortimer, Sahar Mansour

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 303 KB

english, 2008

13

MAST neutral beam long pulse upgrade

S.J. Gee, R. Baldwin, A. Borthwick, D. Ciric, G. Crawford, L. Hackett, D. Homfray, D. Martin, J. Milnes, T. Mutters, M. Simmonds, R. Smith, R. Stephen, P. Stevenson, E. Surrey, C. Waldon, S. Warder, A

Journal:

Fusion Engineering and Design

Year:

2005

Language:

english

File:

PDF, 190 KB

english, 2005

14

Genetic testing is important in families with a history suggestive of hereditary non-polyposis colorectal cancer even if the Amsterdam criteria are not fulfilled

Mr N. E. Beck, I. P. M. Tomlinson, T. Homfray, S. V. Hodgson, C. J. Harocopos, W. F. Bodmer

Journal:

British Journal of Surgery

Year:

1997

Language:

english

File:

PDF, 451 KB

english, 1997

15

Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)

Whittock, Neil V., Izatt, Louise, Mann, Anuska, Homfray, Tessa, Bennett, Christopher, Mansour, Sahar, Hurst, Jane, Fryer, Alan, Saggar, Anand K., Barwell, Julian G., Ellard, Sian, Clayton, Peter T.

Journal:

The Journal of Investigative Dermatology

Year:

2003

Language:

english

File:

PDF, 402 KB

english, 2003

16

Posterior fossa malformation in fetuses: a report of 56 further cases and a review of the literature

F. Forzano, S. Mansour, A. Ierullo, T. Homfray, B. Thilaganathan

Journal:

Prenatal Diagnosis

Year:

2007

Language:

english

File:

PDF, 201 KB

english, 2007

17

Outcome of prenatally diagnosed agenesis of the corpus callosum

N. Fratelli, A. T. Papageorghiou, F. Prefumo, S. Bakalis, T. Homfray, B. Thilaganathan

Journal:

Prenatal Diagnosis

Year:

2007

Language:

english

File:

PDF, 90 KB

english, 2007

18

Parental mosaic trisomy 21 detected following maternal cell contamination of an amniotic fluid specimen from a normal male pregnancy

Melissa L. Street, John C. K. Barber, Tracy A. Boyle, Katrina H. Ellis, Hilary Bullman, Tessa Homfray

Journal:

Prenatal Diagnosis

Year:

2007

Language:

english

File:

PDF, 62 KB

english, 2007

19

Prenatal diagnosis of non-immune hydrops fetalis: what do we tell the parents?

Susana Santo, Sahar Mansour, Basky Thilaganathan, Tessa Homfray, Aris Papageorghiou, Sandra Calvert, Amar Bhide

Journal:

Prenatal Diagnosis

Year:

2011

Language:

english

File:

PDF, 103 KB

english, 2011

20

Prenatal findings on ultrasound and X-ray in a case of overgrowth syndrome associated with increased nuchal translucency

P. Schwärzler, T. Homfray, S. Campbell, Y. Ville

Journal:

Prenatal Diagnosis

Year:

2001

Language:

english

File:

PDF, 143 KB

english, 2001

21

Linkage and sequence analysis indicate thatCCBE1is mutated in recessively inherited generalised lymphatic dysplasia

Fiona Connell, Kamini Kalidas, Pia Ostergaard, Glen Brice, Tessa Homfray, Lesley Roberts, David J. Bunyan, Sally Mitton, Sahar Mansour, Peter Mortimer, Steve Jeffery, Lymphoedema Consortium

Journal:

Year:

2010

Language:

english

File:

PDF, 416 KB

english, 2010

22

Erratum to: Linkage and sequence analysis indicate thatCCBE1is mutated in recessively inherited generalised lymphatic dysplasia

Fiona Connell, Kamini Kalidas, Pia Ostergaard, Glen Brice, Tessa Homfray, Lesley Roberts, David J. Bunyan, Sally Mitton, Sahar Mansour, Peter Mortimer, Steve Jeffery, Lymphoedema Consortium

Journal:

Year:

2010

Language:

english

File:

PDF, 117 KB

english, 2010

23

A novel system for the direct measurement of the electron energy distribution function by Langmuir probe in ion sources

D. Homfray, B. Crowley

Journal:

Fusion Engineering and Design

Year:

2007

Language:

english

File:

PDF, 1.19 MB

english, 2007

24

The JET high frequency pellet injector project

Alain Geraud, M. Dentan, A. Whitehead, P. Butcher, D. Communal, F. Faisse, J. Gedney, G. Gros, D. Guillaume, L. Hackett, V. Hennion, D. Homfray, R. Lucock, J. McKivitt, M. Sibbald, C. Portafaix, J.P.

Journal:

Fusion Engineering and Design

Year:

2007

Language:

english

File:

PDF, 1.10 MB

english, 2007

25

Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis

Gerber, Sylvie, Perrault, Isabelle, Hanein, Sylvain, Barbet, Fabienne, Ducroq, Dominique, Ghazi, Imad, Martin-Coignard, Dominique, Leowski, Corinne, Homfray, Tessa, Dufier, Jean-Louis

Journal:

European Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 533 KB

english, 2001

26

OC154: Pregnancy outcome of antenatally diagnosed agenesis of the corpus callosum

T. Homfray, F. Prefumo, A. Bhide, H. Vandecruys, K. H. Nicolaides, B. Thilaganathan

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2004

Language:

english

File:

PDF, 40 KB

english, 2004

27

P44.17: Second trimester prenatal diagnosis of Cornelia de Lange Syndrome, identification of limb abnormalites with a sinister cause

T. F. R. Homfray, A. Bhide, I. Jeffery, S. Bower

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2007

Language:

english

File:

PDF, 39 KB

english, 2007

28

OP28.06: Prenatal diagnosis of nonimmune hydrops fetalis: what do we tell the parents?

S. F. Santo, T. D. Dias, S. Mansour, T. Homfray, S. Calvert, B. Thilaganathan, A. Bhide

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2010

Language:

english

File:

PDF, 51 KB

english, 2010

29

Late onset microcephaly: failure of prenatal diagnosis

P. Schwärzler, T. Homfray, J.-P. Bernard, J. M. Bland, Y. Ville

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2003

Language:

english

File:

PDF, 76 KB

english, 2003

30

The prenatal diagnosis of Binder syndrome before 24 weeks of gestation: case report

K. Cook, F. Prefumo, F. Presti, T. Homfray, S. Campbell

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2000

Language:

english

File:

PDF, 63 KB

english, 2000

31

Prenatal ultrasound diagnosis of Leroy I cell disease

Dr C. Lees, T. Homfray, K. H. Nicolaides

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2001

Language:

english

File:

PDF, 47 KB

english, 2001

32

Outcome of antenatally diagnosed talipes equinovarus in an unselected obstetric population

S. Bakalis, S. Sairam, T. Homfray, K. Harrington, K. Nicolaides, Dr B. Thilaganathan

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2002

Language:

english

File:

PDF, 144 KB

english, 2002

33

Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm

Doyle, Alexander J, Doyle, Jefferson J, Bessling, Seneca L, Maragh, Samantha, Lindsay, Mark E, Schepers, Dorien, Gillis, Elisabeth, Mortier, Geert, Homfray, Tessa, Sauls, Kimberly, Norris, Russell A,

Journal:

Nature Genetics

Year:

2012

Language:

english

File:

PDF, 1.27 MB

english, 2012

34

Detection of mosaicism for genome imbalance in a cohort of 3,042 clinical cases using an oligonucleotide array CGH platform

Sarah Hoang, JooWook Ahn, Kathy Mann, Sue Bint, Sahar Mansour, Tessa Homfray, Shehla Mohammed, Caroline Mackie Ogilvie

Journal:

European Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 389 KB

english, 2011

35

Real time neutral beam power control on MAST

David A. Homfray, A. Benn, D. Ciric, I. Day, V. Dunkley, D. Keeling, S. Khilar, D. King, R. King, U. Kurutz, D. Payne, M. Simmonds, P. Stevenson, C. Tame

Journal:

Fusion Engineering and Design

Year:

2011

Language:

english

File:

PDF, 731 KB

english, 2011

36

Subtle chromosomal rearrangements in children with unexplained mental retardation

Samantha JL Knight, Regina Regan, Alison Nicod, Sharon W Horsley, Lyndal Kearney, Tessa Homfray, Robin M Winter, Patrick Bolton, Jonathan Flint

Journal:

Year:

1999

Language:

english

File:

PDF, 168 KB

english, 1999

37

Performance of upgraded JET neutral beam injectors

D. Ćirić, A.D. Ash, B. Crowley, I.E. Day, S.J. Gee, L.J. Hackett, D.A. Homfray, I. Jenkins, T.T.C. Jones, D. Keeling, D.B. King, R.F. King, M. Kovari, R. McAdams, E. Surrey, D. Young, J. Zacks

Journal:

Fusion Engineering and Design

Year:

2011

Language:

english

File:

PDF, 224 KB

english, 2011

38

Counseling in fetal medicine: agenesis of the corpus callosum

Santo, S., D'Antonio, F., Homfray, T., Rich, P., Pilu, G., Bhide, A., Thilaganathan, B., Papageorghiou, A. T.

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2012

Language:

english

File:

PDF, 347 KB

english, 2012

39

Activity in the Fusiform Gyrus Predicts Conscious Perception of Rubin's Vase–Face Illusion

Timothy J. Andrews, Denis Schluppeck, Dave Homfray, Paul Matthews, Colin Blakemore

Journal:

Year:

2002

Language:

english

File:

PDF, 365 KB

english, 2002

40

On the Absorption of Gases by Charcoal

Journal:

Proceedings Mathematical Physical & Engineering Sciences

Year:

1910

Language:

english

File:

PDF, 552 KB

english, 1910

41

Development of multi-platform control and instrumentation communications to increase operational reliability – Application to MAST

Homfray, D.A., Deakin, K., Khilar, S., King, R., Payne, D., Simmonds, M.R., Tame, C., Whitehead, B.

Journal:

Fusion Engineering and Design

Year:

2013

Language:

english

File:

PDF, 877 KB

english, 2013

42

Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation

Bhuiyan, Zahurul A., Momenah, Tarek S., Gong, Qiuming, Amin, Ahmad S., Ghamdi, Saleh Al, Carvalho, Julene S., Homfray, Tessa, Mannens, Marcel M.A.M., Zhou, Zhengfeng, Wilde, Arthur A.M.

Journal:

Year:

2008

Language:

english

File:

PDF, 3.20 MB

english, 2008

43

On the Absorption of Gases by Charcoal

Journal:

Proceedings of the Royal Society of London Series A Containing Papers of a Mathematical and Physical Character (1905-1934)

Year:

1910

Language:

english

File:

PDF, 842 KB

english, 1910

44

Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility

Makita, N., Yagihara, N., Crotti, L., Johnson, C. N., Beckmann, B.-M., Roh, M. S., Shigemizu, D., Lichtner, P., Ishikawa, T., Aiba, T., Homfray, T., Behr, E. R., Klug, D., Denjoy, I., Mastantuono, E.,

Journal:

Circulation Cardiovascular Genetics

Year:

2014

Language:

english

File:

PDF, 3.90 MB

english, 2014

45

2.1 Estimation of detection rates of aneuploidy using an approach based on nuchal translucency and non-invasive prenatal testing (NIPT)

Khalil, A., Mahmoodian, N., Kulkarni, A., Homfray, T., Papageorghiou, A., Bhide, A., Thilaganathan, B.

Journal:

Archives of Disease in Childhood - Fetal and Neonatal Edition

Year:

2014

Language:

english

File:

PDF, 73 KB

english, 2014

46

Replacing the Combined Test by Cell-Free DNA Testing in Screening for Trisomies 21, 18 and 13: Impact on the Diagnosis of Other Chromosomal Abnormalities

Syngelaki, Argyro, Pergament, Eugene, Homfray, Tessa, Akolekar, Ranjit, Nicolaides, Kypros H.

Journal:

Fetal Diagnosis and Therapy

Year:

2014

Language:

english

File:

PDF, 409 KB

english, 2014

47

Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy

Groeneweg, Judith A., Ummels, Amber, Mulder, Marcel, Bikker, Hennie, van der Smagt, Jasper J., van Mil, Anneke M., Homfray, Tessa, Post, Jan G., Elvan, Arif, van der Heijden, Jeroen F., Houweling, Arj

Journal:

Year:

2014

Language:

english

File:

PDF, 812 KB

english, 2014

48

Further notes on acetin

Allen, A. H., Homfray, D.

Journal:

The Analyst (Royal Society of Chemistry)

Year:

1891

Language:

english

File:

PDF, 200 KB

english, 1891

49

Characterization of the ITER model negative ion source during long pulse operation

Hemsworth, R. S., Boilson, D., Crowley, B., Homfray, D., de Esch, H. P. L., Krylov, A., Svensson, L.

Journal:

Review of Scientific Instruments

Year:

2006

Language:

english

File:

PDF, 549 KB

english, 2006

50

A KCNQ1 Mutation Causes a High Penetrance for Familial Atrial Fibrillation

BARTOS, DANIEL C., ANDERSON, JEFFREY B., BASTIAENEN, RACHEL, JOHNSON, JONATHAN N., GOLLOB, MICHAEL H., TESTER, DAVID J., BURGESS, DON E., HOMFRAY, TESSA, BEHR, ELIJAH R., ACKERMAN, MICHAEL J., GUICHEN

Journal:

Journal of Cardiovascular Electrophysiology

Year:

2013

Language:

english

File:

PDF, 843 KB

english, 2013

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