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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
October 27, 2016
Stillbirth and intrauterine fetal death: role of routine histopathological placental findings to determine cause of death
J Man, J C Hutchinson, A E Heazell, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
October 27, 2016
Stillbirth and intrauterine fetal death: contemporary demographic features of >1000 cases from an urban population
J Man, J C Hutchinson, M Ashworth, et al.
Research in Developmental Disabilities
|
January 9, 2010
Cognitive modifiability of children with developmental disabilities: a multicentre study using Feuerstein's Instrumental Enrichment--Basic program
A Kozulin, J Lebeer, A Madella-Noja, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
October 27, 2016
Organ weights and ratios for postmortem identification of fetal growth restriction: utility and confounding factors
J Man, J C Hutchinson, M Ashworth, et al.
Journal of Clinical Pathology
|
January 1, 1983
Prognostic value of tumour thickness in cutaneous malignant melanoma
I Jeffrey, P Royston, C Sowter, et al.
The Histochemical Journal
|
February 18, 1998
Polycystin expression during embryonic development of human kidney in adult tissues and ADPKD tissue
B S Weston, S Jeffery, I Jeffrey, et al.
Nucleic Acids Research
|
September 25, 1993
Comparative analysis of the regulation of the interferon-inducible protein kinase PKR by Epstein-Barr virus RNAs EBER-1 and EBER-2 and adenovirus VAI RNA
T V Sharp, M Schwemmle, I Jeffrey, et al.
Clinical Genetics
|
January 14, 2012
CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis
F C Connell, K Kalidas, P Ostergaard, et al.
Journal of Medical Genetics
|
December 20, 2003
Greenberg dysplasia (HEM) and lethal X linked dominant Conradi-Hünermann chondrodysplasia punctata (CDPX2): presentation of two cases with overlapping phenotype
A C Offiah, S Mansour, I Jeffrey, et al.
Plos One
|
March 13, 2015
Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease
Terry D Heiman-Patterson, Elizabeth P Blankenhorn, Roger B Sher, et al.
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Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
October 27, 2016
Stillbirth and intrauterine fetal death: role of routine histopathological placental findings to determine cause of death
J Man, J C Hutchinson, A E Heazell, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
October 27, 2016
Stillbirth and intrauterine fetal death: contemporary demographic features of >1000 cases from an urban population
J Man, J C Hutchinson, M Ashworth, et al.
Research in Developmental Disabilities
|
January 9, 2010
Cognitive modifiability of children with developmental disabilities: a multicentre study using Feuerstein's Instrumental Enrichment--Basic program
A Kozulin, J Lebeer, A Madella-Noja, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
October 27, 2016
Organ weights and ratios for postmortem identification of fetal growth restriction: utility and confounding factors
J Man, J C Hutchinson, M Ashworth, et al.
Journal of Clinical Pathology
|
January 1, 1983
Prognostic value of tumour thickness in cutaneous malignant melanoma
I Jeffrey, P Royston, C Sowter, et al.
The Histochemical Journal
|
February 18, 1998
Polycystin expression during embryonic development of human kidney in adult tissues and ADPKD tissue
B S Weston, S Jeffery, I Jeffrey, et al.
Nucleic Acids Research
|
September 25, 1993
Comparative analysis of the regulation of the interferon-inducible protein kinase PKR by Epstein-Barr virus RNAs EBER-1 and EBER-2 and adenovirus VAI RNA
T V Sharp, M Schwemmle, I Jeffrey, et al.
Clinical Genetics
|
January 14, 2012
CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis
F C Connell, K Kalidas, P Ostergaard, et al.
Journal of Medical Genetics
|
December 20, 2003
Greenberg dysplasia (HEM) and lethal X linked dominant Conradi-Hünermann chondrodysplasia punctata (CDPX2): presentation of two cases with overlapping phenotype
A C Offiah, S Mansour, I Jeffrey, et al.
Plos One
|
March 13, 2015
Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease
Terry D Heiman-Patterson, Elizabeth P Blankenhorn, Roger B Sher, et al.
Page
of 4