Search research articles
Contact Us
Filters
Showing results (41-50 of 45) with videos related to
Page
of 5
Sort By:
You have reached the last page of results.
This site can display upto 45 results.
Transplant Infectious Disease : an Official Journal of the Transplantation Society
|
January 14, 2022
Impact of COVID-19 in hematopoietic stem cell transplant recipients: A systematic review and meta-analysis
Moazzam Shahzad, Sibgha Gull Chaudhary, Muhammad U Zafar, et al.
American Journal of Human Genetics
|
December 31, 2005
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness
Saima Riazuddin, Shaheen N Khan, Zubair M Ahmed, et al.
Human Mutation
|
January 9, 2008
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function
Saima Riazuddin, Sabiha Nazli, Zubair M Ahmed, et al.
American Journal of Human Genetics
|
September 21, 2010
A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness
S Amer Riazuddin, Amber Shahzadi, Christina Zeitz, et al.
The Lancet. HIV
|
April 5, 2026
Pitavastatin effects on lipids in relation to major adverse cardiovascular events: a REPRIEVE secondary analysis
Triin Umbleja, Mohammad U Zafar, Sara McCallum, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 45) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 45 results.
Transplant Infectious Disease : an Official Journal of the Transplantation Society
|
January 14, 2022
Impact of COVID-19 in hematopoietic stem cell transplant recipients: A systematic review and meta-analysis
Moazzam Shahzad, Sibgha Gull Chaudhary, Muhammad U Zafar, et al.
American Journal of Human Genetics
|
December 31, 2005
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness
Saima Riazuddin, Shaheen N Khan, Zubair M Ahmed, et al.
Human Mutation
|
January 9, 2008
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function
Saima Riazuddin, Sabiha Nazli, Zubair M Ahmed, et al.
American Journal of Human Genetics
|
September 21, 2010
A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness
S Amer Riazuddin, Amber Shahzadi, Christina Zeitz, et al.
The Lancet. HIV
|
April 5, 2026
Pitavastatin effects on lipids in relation to major adverse cardiovascular events: a REPRIEVE secondary analysis
Triin Umbleja, Mohammad U Zafar, Sara McCallum, et al.
Page
of 5