Denise Williams
发表
Alessandro,
G. J. Swaminathan,
A. Green,
2019
.
S. Weremowicz,
C. Morton,
C. Eng,
1999
.
G. Ravenscroft,
E. Todd,
N. Romero,
2015,
Orphanet Journal of Rare Diseases.
A. Uyttebroeck,
L. Brugières,
A. Reiter,
2013,
Pediatric blood & cancer.
A. Attarbaschi,
K. Horibe,
A. Uyttebroeck,
2010,
Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
K. Horibe,
A. Uyttebroeck,
L. Brugières,
2009,
Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
Bethan E. Hoskins,
P. Beales,
D. Milford,
2017,
Journal of the American Society of Nephrology : JASN.
M. Kilby,
E. Quinlan-Jones,
T. Marton,
2020,
Prenatal diagnosis.
G. Delsol,
L. Brugières,
K. McCarthy,
2008,
Blood.
J. Macdougall,
A. Prakash,
Denise Williams,
2016
.
Mark T. Handley,
J. Graham,
F. Müller,
2011,
American journal of human genetics.
Jay F Rowland,
M. Hurles,
Soo-Mi Park,
2019,
The Lancet.
R. Finkel,
P. Bauer,
M. Baudis,
2013,
Brain : a journal of neurology.
D. Lomas,
N. Twyman,
N. Burnet,
2003,
Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.
M. Tarnopolsky,
A. Fry,
S. Davies,
2020,
American journal of human genetics.
B. Burkhardt,
A. Attarbaschi,
A. Uyttebroeck,
2016,
Haematologica.
A. de la Chapelle,
S. Tuft,
S. Bhattacharya,
2007,
Molecular vision.
K. Horibe,
L. Brugières,
A. Mauguen,
2011,
Pediatric blood & cancer.
G. Levitt,
P. Crofton,
Denise Williams,
2008,
Pediatric blood & cancer.
J. Hewitt,
T. Cole,
S. Clokie,
2016,
Prenatal diagnosis.
J. Hewitt,
T. Cole,
S. Clokie,
2017,
European Journal of Human Genetics.
M. Kilby,
E. Kinning,
Denise Williams,
2022,
Genes.
M. Kilby,
T. Marton,
F. Mone,
2020,
Acta obstetricia et gynecologica Scandinavica.
R. Morris,
M. Kilby,
E. Quinlan-Jones,
2019,
Prenatal diagnosis.
A. Gerrish,
J. Hewitt,
T. Cole,
2020,
The Journal of molecular diagnostics : JMD.
M. Kilby,
E. Quinlan-Jones,
C. Bell,
2016,
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
A. Fry,
K. Lachlan,
R. Newbury-Ecob,
2020,
American journal of medical genetics. Part A.
Denise Williams,
R. Palmer,
2003,
Medical and pediatric oncology.
J. Clayton-Smith,
B. Lorenz,
I. Temple,
2016,
PloS one.
Tomas W. Fitzgerald,
G. J. Swaminathan,
J. Danesh,
2016,
Nature Genetics.
M. Hurles,
M. Kilby,
E. Prigmore,
2018,
Genetics in Medicine.
C. Fallet-Bianco,
C. Ricketts,
R. Trembath,
2010,
American journal of human genetics.
L. Brueton,
D. Lim,
D. McMullan,
2014,
American journal of medical genetics. Part A.
Joan,
Caroline,
Rajan,
2017,
Nature.
Patrick J. Short,
M. Hurles,
L. Vissers,
2020,
Nature.
Joshua C Randall,
Tomas W. Fitzgerald,
G. J. Swaminathan,
2016,
bioRxiv.
Joshua C Randall,
G. J. Swaminathan,
A. Green,
2019
.
M. Hurles,
R. Sandford,
D. Baralle,
2020,
Nature Communications.
D. Bonthron,
G. Taylor,
E. Sheridan,
2009,
Human mutation.
V. Tillmann,
F. Urano,
T. Hershey,
2017,
Human mutation.
P. Yu-Wai-Man,
N. Beer,
T. Barrett,
2021,
Journal of Medical Genetics.
W. Klapper,
B. Burkhardt,
S. Perkins,
2015,
Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
M. Kilby,
Denise Williams,
S. Allen,
2021,
Expert review of molecular diagnostics.
J. Gupta,
Denise Williams,
V. Hodgetts,
2010,
European journal of obstetrics, gynecology, and reproductive biology.
N. Rahman,
S. Hanks,
A. Craft,
2008,
Nature Genetics.
K. C. Morris,
E. Quinlan-Jones,
T. Marton,
2017,
Clinical case reports.
I. Judson,
N. Carroll,
M. Murray,
2008,
Pediatric blood & cancer.
A. Attarbaschi,
K. Horibe,
A. Uyttebroeck,
2011,
Blood.
E. Tobias,
B. Lorenz,
J. Hurst,
2019,
Genetics in Medicine.
Prenatal thoraco-amniotic chest drain insertion to manage a case of fetal hydrops secondary to FOXC2
R. Morris,
M. Kilby,
Nidhi Gulati,
2018,
BMJ Case Reports.
T. de Ravel,
I. Casteels,
G. Arno,
2020,
Scientific Reports.
C. Romano,
E. Eichler,
H. Firth,
2020,
Genetics in Medicine.
M. Kilby,
Denise Williams,
S. Allen,
2019,
Genetics research.
D. Wieczorek,
S. Mansour,
A. Moore,
2013,
European Journal of Human Genetics.
A. Munnich,
K. Devriendt,
R. Hennekam,
2011,
Journal of Medical Genetics.
Asif Javed,
Shifeng Xue,
H. Kayserili,
2017,
Nature Genetics.
W. Klapper,
B. Burkhardt,
S. Turner,
2020,
Cancers.
Sian Ellard,
Andrew T. Hattersley,
A. Hattersley,
2010,
Diabetes.
Nazneen Rahman,
Neil J. Sebire,
Kathy Pritchard-Jones,
2012,
Oncotarget.
S. Seal,
N. Rahman,
S. Hanks,
2019,
The Lancet. Child & adolescent health.
C. Fallet-Bianco,
T. Marton,
C. Patel,
2010,
American journal of medical genetics. Part A.
Joshua C Randall,
Tomas W. Fitzgerald,
G. J. Swaminathan,
2018,
Nature Communications.
B. Burkhardt,
A. Attarbaschi,
A. Uyttebroeck,
2013,
Annals of Hematology.
Tomas W. Fitzgerald,
G. J. Swaminathan,
J. Danesh,
2016
.
J. Ainsworth,
Denise Williams,
G. Kirkby,
2008,
Ophthalmic genetics.
Robert W. Taylor,
Mark T. Handley,
A. von Kriegsheim,
2019,
PLoS genetics.
Robert W. Taylor,
Mark T. Handley,
A. von Kriegsheim,
2018,
bioRxiv.
L. Brugières,
A. Reiter,
M. Deley,
2006
.
H. Earl,
N. Burnet,
G. Horan,
2009,
Pediatric blood & cancer.
Joshua C Randall,
Tomas W. Fitzgerald,
G. J. Swaminathan,
2018,
American journal of human genetics.
M. Kilby,
D. McMullan,
F. Mackie,
2017,
Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.
M. Kilby,
D. McMullan,
F. Mackie,
2014,
Prenatal diagnosis.
K. C. Morris,
E. Quinlan-Jones,
T. Marton,
2017,
Clinical case reports.
Mark T. Handley,
J. Graham,
F. Müller,
2011,
American journal of human genetics.