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K Temple

Showing results (241-250 of 262) with videos related to

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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 amplificationJ 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 cancerB 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 mellitusD 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 panelJinru 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 MarkersTsuyoshi 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 chemoradiotherapyJinru Shia, Martine McManus, Jose G Guillem, et al.
European Radiology|August 28, 2013
Prognostic aspects of DCE-MRI in recurrent rectal cancerM 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 lifespanJocelynn 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 effectP 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 patientsGuillaume Jedraszak, Bénédicte Demeer, Michèle Mathieu-Dramard, et al.
Pageof 27

Showing results (241-250 of 262) with videos related to

Sort By:
Pageof 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 amplificationJ 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 cancerB 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 mellitusD 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 panelJinru 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 MarkersTsuyoshi 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 chemoradiotherapyJinru Shia, Martine McManus, Jose G Guillem, et al.
European Radiology|August 28, 2013
Prognostic aspects of DCE-MRI in recurrent rectal cancerM 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 lifespanJocelynn 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 effectP 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 patientsGuillaume Jedraszak, Bénédicte Demeer, Michèle Mathieu-Dramard, et al.
Pageof 27