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Transplantation Proceedings
|
November 14, 2006
Early postoperative response of cytokines in liver transplant recipients
L Hassan, P Bueno, I Ferrón-Celma, et al.
American Journal of Medical Genetics. Part A
|
January 21, 2016
Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts
Julia E VanderMeer, Tonia C Carter, Faith Pangilinan, et al.
American Journal of Human Genetics
|
May 10, 2011
Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome
James O'Sullivan, Carolina C Bitu, Sarah B Daly, et al.
American Journal of Medical Genetics. Part A
|
May 17, 2011
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome
Nicholas K Rorick, Akira Kinoshita, Jason L Weirather, et al.
Human Genetics
|
March 21, 2013
Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study
T H Beaty, M A Taub, A F Scott, et al.
Journal of Medical Genetics
|
September 18, 2007
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation
K Osoegawa, G M Vessere, K H Utami, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
July 12, 2011
Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders
A Butali, P A Mossey, W L Adeyemo, et al.
Nature Genetics
|
May 4, 2010
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
Terri H Beaty, Jeffrey C Murray, Mary L Marazita, et al.
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Search research articles
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Showing results (41-50 of 48) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 48 results.
Transplantation Proceedings
|
November 14, 2006
Early postoperative response of cytokines in liver transplant recipients
L Hassan, P Bueno, I Ferrón-Celma, et al.
American Journal of Medical Genetics. Part A
|
January 21, 2016
Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts
Julia E VanderMeer, Tonia C Carter, Faith Pangilinan, et al.
American Journal of Human Genetics
|
May 10, 2011
Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome
James O'Sullivan, Carolina C Bitu, Sarah B Daly, et al.
American Journal of Medical Genetics. Part A
|
May 17, 2011
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome
Nicholas K Rorick, Akira Kinoshita, Jason L Weirather, et al.
Human Genetics
|
March 21, 2013
Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study
T H Beaty, M A Taub, A F Scott, et al.
Journal of Medical Genetics
|
September 18, 2007
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation
K Osoegawa, G M Vessere, K H Utami, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
July 12, 2011
Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders
A Butali, P A Mossey, W L Adeyemo, et al.
Nature Genetics
|
May 4, 2010
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
Terri H Beaty, Jeffrey C Murray, Mary L Marazita, et al.
Page
of 5