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Bone
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August 4, 2009
Vitamin D receptor gene polymorphisms modulate the skeletal response to vitamin D supplementation in healthy girls
Asma Arabi, Laila Zahed, Ziyad Mahfoud, et al.
American Journal of Medical Genetics. Part A
|
February 28, 2008
Molecular and clinical description of a girl with a 46,X,t(Y;4)(q11.2;p16)/45,X,der(4)t(Y;4)(q11.2;p16) karyotype and a small cryptic 4p subtelomeric deletion
Laila Zahed, Carolina Sismani, M Ioannides, et al.
American Journal of Human Genetics
|
June 15, 2006
Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure
Arnaud Lacombe, Hane Lee, Laila Zahed, et al.
American Journal of Hematology
|
April 29, 2010
Vascular at-risk genotypes and disease severity in Lebanese sickle cell disease patients
Chantal Farra, Laila Zahed, Paul J Nietert, et al.
Human Mutation
|
November 16, 2019
DNA repair functional analyses of NBN hypomorphic variants associated with NBN-related infertility
Alice Fiévet, Dorine Bellanger, Laila Zahed, et al.
Blood
|
June 7, 2006
Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I
Momin R Ahmed, Aref Chehal, Laila Zahed, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 16 results.
Bone
|
August 4, 2009
Vitamin D receptor gene polymorphisms modulate the skeletal response to vitamin D supplementation in healthy girls
Asma Arabi, Laila Zahed, Ziyad Mahfoud, et al.
American Journal of Medical Genetics. Part A
|
February 28, 2008
Molecular and clinical description of a girl with a 46,X,t(Y;4)(q11.2;p16)/45,X,der(4)t(Y;4)(q11.2;p16) karyotype and a small cryptic 4p subtelomeric deletion
Laila Zahed, Carolina Sismani, M Ioannides, et al.
American Journal of Human Genetics
|
June 15, 2006
Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure
Arnaud Lacombe, Hane Lee, Laila Zahed, et al.
American Journal of Hematology
|
April 29, 2010
Vascular at-risk genotypes and disease severity in Lebanese sickle cell disease patients
Chantal Farra, Laila Zahed, Paul J Nietert, et al.
Human Mutation
|
November 16, 2019
DNA repair functional analyses of NBN hypomorphic variants associated with NBN-related infertility
Alice Fiévet, Dorine Bellanger, Laila Zahed, et al.
Blood
|
June 7, 2006
Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I
Momin R Ahmed, Aref Chehal, Laila Zahed, et al.
Page
of 2