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Journal of Medical Genetics
|
September 6, 2005
Partial NSD1 deletions cause 5% of Sotos syndrome and are readily identifiable by multiplex ligation dependent probe amplification
J Douglas, K Tatton-Brown, K Coleman, et al.
Human Genetics
|
April 6, 1999
Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer
B V Bapat, L Madlensky, L K Temple, et al.
Human Genetics
|
January 13, 2006
Epimutation of the TNDM locus and the Beckwith-Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus
D J G Mackay, J M D Hahnemann, S E Boonen, et al.
The American Journal of Surgical Pathology
|
August 25, 2009
Immunohistochemistry as first-line screening for detecting colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: a 2-antibody panel may be as predictive as a 4-antibody panel
Jinru Shia, Laura H Tang, Efsevia Vakiani, et al.
The American Journal of Surgical Pathology
|
April 7, 2018
Poorly Differentiated Clusters Predict Colon Cancer Recurrence: An In-Depth Comparative Analysis of Invasive-Front Prognostic Markers
Tsuyoshi Konishi, Yoshifumi Shimada, Lik Hang Lee, et al.
The American Journal of Surgical Pathology
|
December 18, 2010
Significance of acellular mucin pools in rectal carcinoma after neoadjuvant chemoradiotherapy
Jinru Shia, Martine McManus, Jose G Guillem, et al.
European Radiology
|
August 28, 2013
Prognostic aspects of DCE-MRI in recurrent rectal cancer
M J Gollub, K Cao, D H Gultekin, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
December 16, 2015
Fetal alcohol spectrum disorder: a guideline for diagnosis across the lifespan
Jocelynn L Cook, Courtney R Green, Christine M Lilley, et al.
Journal of Medical Genetics
|
February 4, 2005
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect
P Brouillard, M Ghassibé, A Penington, et al.
American Journal of Medical Genetics. Part A
|
January 10, 2015
Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: six new patients
Guillaume Jedraszak, Bénédicte Demeer, Michèle Mathieu-Dramard, et al.
Page
of 27
Search research articles
Search
Showing results (241-250 of 262) with videos related to
Sort By:
Page
of 27
Journal of Medical Genetics
|
September 6, 2005
Partial NSD1 deletions cause 5% of Sotos syndrome and are readily identifiable by multiplex ligation dependent probe amplification
J Douglas, K Tatton-Brown, K Coleman, et al.
Human Genetics
|
April 6, 1999
Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer
B V Bapat, L Madlensky, L K Temple, et al.
Human Genetics
|
January 13, 2006
Epimutation of the TNDM locus and the Beckwith-Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus
D J G Mackay, J M D Hahnemann, S E Boonen, et al.
The American Journal of Surgical Pathology
|
August 25, 2009
Immunohistochemistry as first-line screening for detecting colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: a 2-antibody panel may be as predictive as a 4-antibody panel
Jinru Shia, Laura H Tang, Efsevia Vakiani, et al.
The American Journal of Surgical Pathology
|
April 7, 2018
Poorly Differentiated Clusters Predict Colon Cancer Recurrence: An In-Depth Comparative Analysis of Invasive-Front Prognostic Markers
Tsuyoshi Konishi, Yoshifumi Shimada, Lik Hang Lee, et al.
The American Journal of Surgical Pathology
|
December 18, 2010
Significance of acellular mucin pools in rectal carcinoma after neoadjuvant chemoradiotherapy
Jinru Shia, Martine McManus, Jose G Guillem, et al.
European Radiology
|
August 28, 2013
Prognostic aspects of DCE-MRI in recurrent rectal cancer
M J Gollub, K Cao, D H Gultekin, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
December 16, 2015
Fetal alcohol spectrum disorder: a guideline for diagnosis across the lifespan
Jocelynn L Cook, Courtney R Green, Christine M Lilley, et al.
Journal of Medical Genetics
|
February 4, 2005
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect
P Brouillard, M Ghassibé, A Penington, et al.
American Journal of Medical Genetics. Part A
|
January 10, 2015
Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: six new patients
Guillaume Jedraszak, Bénédicte Demeer, Michèle Mathieu-Dramard, et al.
Page
of 27