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Journal of Acquired Immune Deficiency Syndromes (1999)
|
July 29, 2021
Identifying Missed Opportunities in the Prevention of Acute HIV Infection: The Need to Provide Pre-exposure Prophylaxis Referrals to Emergency Department Patients With Increased Risk for Acquiring HIV
Noah W Schlenker, Nathan A Irvin, Giorgio G Galetto, et al.
American Journal of Human Genetics
|
October 30, 1998
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1
D Johnson, S W Horsley, D M Moloney, et al.
The Laryngoscope
|
November 2, 2024
Prostaglandin E Receptor 2 (EP2) Dysregulation in Allergic Fungal Rhinosinusitis Nasal Polyp Epithelium
Prestina Smith-Davidson, Khaled Altartoor, M M Kabongo, et al.
Clinical Genetics
|
October 2, 2009
Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders
H M Ozgen, E van Daalen, P F Bolton, et al.
Advances in Experimental Medicine and Biology
|
May 9, 2008
Nebraska experience
S R Walker, J C Lund, D G Schumacher, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties
|
December 20, 2022
Specimen-Based Resection Margins and Local Control during Transoral Robotic Surgery for Oropharyngeal HPV-Mediated Squamous Cell Carcinoma
Kelly R Magliocca, Azeem S Kaka, Emily M Barrow, et al.
The Journal of Pathology
|
August 10, 2017
Smoking is associated with hypermethylation of the APC 1A promoter in colorectal cancer: the ColoCare Study
Timothy M Barrow, Hagen Klett, Reka Toth, et al.
Journal of Medical Genetics
|
February 4, 2005
The importance of seeking ALMS1 mutations in infants with dilated cardiomyopathy
J Bond, K Flintoff, J Higgins, et al.
Human Mutation
|
October 16, 2007
Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families
B L Callewaert, A Willaert, W S Kerstjens-Frederikse, et al.
American Journal of Human Genetics
|
April 6, 2000
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene
D M Hagan, A J Ross, T Strachan, et al.
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of 11
Search research articles
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Showing results (101-110 of 110) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 110 results.
Journal of Acquired Immune Deficiency Syndromes (1999)
|
July 29, 2021
Identifying Missed Opportunities in the Prevention of Acute HIV Infection: The Need to Provide Pre-exposure Prophylaxis Referrals to Emergency Department Patients With Increased Risk for Acquiring HIV
Noah W Schlenker, Nathan A Irvin, Giorgio G Galetto, et al.
American Journal of Human Genetics
|
October 30, 1998
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1
D Johnson, S W Horsley, D M Moloney, et al.
The Laryngoscope
|
November 2, 2024
Prostaglandin E Receptor 2 (EP2) Dysregulation in Allergic Fungal Rhinosinusitis Nasal Polyp Epithelium
Prestina Smith-Davidson, Khaled Altartoor, M M Kabongo, et al.
Clinical Genetics
|
October 2, 2009
Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders
H M Ozgen, E van Daalen, P F Bolton, et al.
Advances in Experimental Medicine and Biology
|
May 9, 2008
Nebraska experience
S R Walker, J C Lund, D G Schumacher, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties
|
December 20, 2022
Specimen-Based Resection Margins and Local Control during Transoral Robotic Surgery for Oropharyngeal HPV-Mediated Squamous Cell Carcinoma
Kelly R Magliocca, Azeem S Kaka, Emily M Barrow, et al.
The Journal of Pathology
|
August 10, 2017
Smoking is associated with hypermethylation of the APC 1A promoter in colorectal cancer: the ColoCare Study
Timothy M Barrow, Hagen Klett, Reka Toth, et al.
Journal of Medical Genetics
|
February 4, 2005
The importance of seeking ALMS1 mutations in infants with dilated cardiomyopathy
J Bond, K Flintoff, J Higgins, et al.
Human Mutation
|
October 16, 2007
Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families
B L Callewaert, A Willaert, W S Kerstjens-Frederikse, et al.
American Journal of Human Genetics
|
April 6, 2000
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene
D M Hagan, A J Ross, T Strachan, et al.
Page
of 11