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Showing results (1131-1140 of 1,465) with videos related to

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JAMA Pediatrics|July 2, 2016
Prevention of Congenital Disorders and Care of Affected Children: A Consensus StatementGary L Darmstadt, Christopher P Howson, Gijs Walraven, et al.
Genes|August 28, 2025
Gene-by-Environment Interactions Involving Maternal Exposures with Orofacial Cleft Risk in FilipinosZeynep Erdogan-Yildirim, Jenna C Carlson, Nandita Mukhopadhyay, et al.
Investigational New Drugs|December 29, 2010
Effect of hepatic or renal impairment on the pharmacokinetics of casopitant, a NK-1 receptor antagonistJohn W Bauman, Joyce M Antal, Laurel M Adams, et al.
Human Molecular Genetics|May 1, 1994
Localization of the achondroplasia gene to the distal 2.5 Mb of human chromosome 4pC A Francomano, R I Ortiz de Luna, T W Hefferon, et al.
Australian Journal of Ophthalmology|February 1, 1984
The FDA report on intraocular lensesW J Stark, D M Worthen, J T Holladay, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Rare genetic variants in <i>SEC24D</i> modify orofacial cleft phenotypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
Clinical Genetics|July 30, 2013
Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypesE Weh, L M Reis, R C Tyler, et al.
Journal of Perinatal Medicine|May 15, 2013
Periconceptional use of folic acid and risk of miscarriage - findings of the Oral Cleft Prevention Program in BrazilCamila Vila-Nova, George L Wehby, Fernanda C Queirós, et al.
Gene Expression|January 5, 2002
Antagonistic regulation of Dlx2 expression by PITX2 and Msx2: implications for tooth developmentP D Green, T A Hjalt, D E Kirk, et al.
Nature Genetics|October 17, 2006
Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)Christopher R Ingraham, Akira Kinoshita, Shinji Kondo, et al.
Pageof 147

Showing results (1131-1140 of 1,465) with videos related to

Sort By:
Pageof 147
JAMA Pediatrics|July 2, 2016
Prevention of Congenital Disorders and Care of Affected Children: A Consensus StatementGary L Darmstadt, Christopher P Howson, Gijs Walraven, et al.
Genes|August 28, 2025
Gene-by-Environment Interactions Involving Maternal Exposures with Orofacial Cleft Risk in FilipinosZeynep Erdogan-Yildirim, Jenna C Carlson, Nandita Mukhopadhyay, et al.
Investigational New Drugs|December 29, 2010
Effect of hepatic or renal impairment on the pharmacokinetics of casopitant, a NK-1 receptor antagonistJohn W Bauman, Joyce M Antal, Laurel M Adams, et al.
Human Molecular Genetics|May 1, 1994
Localization of the achondroplasia gene to the distal 2.5 Mb of human chromosome 4pC A Francomano, R I Ortiz de Luna, T W Hefferon, et al.
Australian Journal of Ophthalmology|February 1, 1984
The FDA report on intraocular lensesW J Stark, D M Worthen, J T Holladay, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Rare genetic variants in <i>SEC24D</i> modify orofacial cleft phenotypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
Clinical Genetics|July 30, 2013
Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypesE Weh, L M Reis, R C Tyler, et al.
Journal of Perinatal Medicine|May 15, 2013
Periconceptional use of folic acid and risk of miscarriage - findings of the Oral Cleft Prevention Program in BrazilCamila Vila-Nova, George L Wehby, Fernanda C Queirós, et al.
Gene Expression|January 5, 2002
Antagonistic regulation of Dlx2 expression by PITX2 and Msx2: implications for tooth developmentP D Green, T A Hjalt, D E Kirk, et al.
Nature Genetics|October 17, 2006
Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)Christopher R Ingraham, Akira Kinoshita, Shinji Kondo, et al.
Pageof 147