Search research articles
Contact Us
Filters
Showing results (31-40 of 55) with videos related to
Page
of 6
Sort By:
Clinical Dysmorphology
|
April 1, 1994
Prenatal ultrasound findings in a fetus with otopalatodigital syndrome type II
D M Eccles, I E Moore, S Cook, et al.
Journal of Medical Genetics
|
September 1, 2010
A novel HER2-positive breast cancer phenotype arising from germline TP53 mutations
J R F Wilson, A C Bateman, H Hanson, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
July 9, 2015
BRCA1 and BRCA2 genetic testing-pitfalls and recommendations for managing variants of uncertain clinical significance
D M Eccles, G Mitchell, A N A Monteiro, et al.
Journal of Medical Genetics
|
June 3, 2004
A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO
D G R Evans, D M Eccles, N Rahman, et al.
Journal of Medical Genetics
|
April 1, 1994
Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion
J C Barber, K H Ellis, L V Bowles, et al.
Clinical Dysmorphology
|
April 1, 1995
Craniofacial abnormalities, agenesis of the corpus callosum, polysyndactyly and abnormal skin and gut development--the Curry Jones syndrome
I K Temple, D M Eccles, R M Winter, et al.
British Journal of Cancer
|
August 1, 1995
Chromosome 11 allele imbalance and clinicopathological correlates in ovarian tumours
H Gabra, L Taylor, B B Cohen, et al.
Archives of Disease in Childhood
|
March 6, 1998
An unusually severe phenotype for familial adenomatous polyposis
D M Eccles, P W Lunt, Y Wallis, et al.
Cancer Chemotherapy and Pharmacology
|
January 1, 1991
Mitozantrone and prednimustine in the treatment of advanced breast cancer--a toxic regimen with low activity
M E O'Brien, D M Eccles, S G Allen, et al.
Cancer Research
|
May 1, 1993
p53 mutation is a common genetic event in ovarian carcinoma
B J Milner, L A Allan, D M Eccles, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 55) with videos related to
Sort By:
Page
of 6
Clinical Dysmorphology
|
April 1, 1994
Prenatal ultrasound findings in a fetus with otopalatodigital syndrome type II
D M Eccles, I E Moore, S Cook, et al.
Journal of Medical Genetics
|
September 1, 2010
A novel HER2-positive breast cancer phenotype arising from germline TP53 mutations
J R F Wilson, A C Bateman, H Hanson, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
July 9, 2015
BRCA1 and BRCA2 genetic testing-pitfalls and recommendations for managing variants of uncertain clinical significance
D M Eccles, G Mitchell, A N A Monteiro, et al.
Journal of Medical Genetics
|
June 3, 2004
A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO
D G R Evans, D M Eccles, N Rahman, et al.
Journal of Medical Genetics
|
April 1, 1994
Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion
J C Barber, K H Ellis, L V Bowles, et al.
Clinical Dysmorphology
|
April 1, 1995
Craniofacial abnormalities, agenesis of the corpus callosum, polysyndactyly and abnormal skin and gut development--the Curry Jones syndrome
I K Temple, D M Eccles, R M Winter, et al.
British Journal of Cancer
|
August 1, 1995
Chromosome 11 allele imbalance and clinicopathological correlates in ovarian tumours
H Gabra, L Taylor, B B Cohen, et al.
Archives of Disease in Childhood
|
March 6, 1998
An unusually severe phenotype for familial adenomatous polyposis
D M Eccles, P W Lunt, Y Wallis, et al.
Cancer Chemotherapy and Pharmacology
|
January 1, 1991
Mitozantrone and prednimustine in the treatment of advanced breast cancer--a toxic regimen with low activity
M E O'Brien, D M Eccles, S G Allen, et al.
Cancer Research
|
May 1, 1993
p53 mutation is a common genetic event in ovarian carcinoma
B J Milner, L A Allan, D M Eccles, et al.
Page
of 6