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Circulation Research|February 16, 2013
Genetics of congenital heart disease: the glass half emptyAkl C Fahed, Bruce D Gelb, J G Seidman, et al.The Journal of Biological Chemistry|August 28, 2001
Cloning and characterization of a novel mouse AP-2 transcription factor, AP-2delta, with unique DNA binding and transactivation propertiesF Zhao, M Satoda, J D Licht, et al.European Journal of Human Genetics : EJHG|April 12, 2021
Biallelic loss-of-function variants in KCNJ16 presenting with hypokalemic metabolic acidosisBryn D Webb, Hilary Hotchkiss, Pankaj Prasun, et al.Journal of Virology|October 1, 1973
Reassortment of simian virus 40 DNA during serial undiluted passageM A Martin, L D Gelb, G C Fareed, et al.Nature Genetics|July 3, 1999
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndromeG A Diaz, M Banikazemi, K Oishi, et al.American Journal of Medical Genetics|December 5, 2000
Char syndrome: an additional family with polythelia, a new findingR Zannolli, R Mostardini, M Matera, et al.Developmental Biology|January 24, 2004
Male infertility due to germ cell apoptosis in mice lacking the thiamin carrier, Tht1. A new insight into the critical role of thiamin in spermatogenesisKimihiko Oishi, Marco Barchi, Audrey C Au, et al.Neurosurgery|December 1, 1988
Presentation of type I Chiari malformation after head traumaT J Mampalam, B T Andrews, D Gelb, et al.Genome Medicine|January 17, 2020
De novo variants in exomes of congenital heart disease patients identify risk genes and pathwaysCigdem Sevim Bayrak, Peng Zhang, Martin Tristani-Firouzi, et al.Genes, Chromosomes & Cancer|December 29, 1999
Malignant fibrous histiocytoma: inherited and sporadic forms have loss of heterozygosity at chromosome bands 9p21-22-evidence for a common genetic defectJ A Martignetti, B D Gelb, H Pierce, et al.Pageof 39