Sökresultat - Gelb, Bruce D.

Recent advances in understanding the genetics of congenital heart defects av Gelb, Bruce D.

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History of Our Understanding of the Causes of Congenital Heart Disease av Gelb, Bruce D.

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The Hole and the Whole: Lessons from Manipulation of Nipbl Deficiency av Gelb, Bruce D.

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Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanisms av Tartaglia, Marco, Gelb, Bruce D.

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RAS signaling pathway mutations and hypertrophic cardiomyopathy: getting into and out of the thick of it av Gelb, Bruce D., Tartaglia, Marco

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Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment av Linglart, Léa, Gelb, Bruce D.

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A de novo pathogenic BMP2 variant-related phenotype with the novel finding of bicuspid aortic valve av Ahluwalia, Neha, Gelb, Bruce D.

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The Good SHP2 Association: A Porthole into the Genetics of Congenital Heart Disease av Gelb, Bruce D., Seidman, Christine E.

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Concise Review: Drug Discovery in the Age of the Induced Pluripotent Stem Cell av Ko, Huaising C., Gelb, Bruce D.

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Complex Genetics and the Etiology of Human Congenital Heart Disease av Gelb, Bruce D., Chung, Wendy K.

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Genetics of congenital heart disease av Edwards, Jonathan J., Gelb, Bruce D.

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Noonan syndrome and clinically related disorders av Tartaglia, Marco, Gelb, Bruce D., Zenker, Martin

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Cardiomyopathies in Noonan syndrome and the other RASopathies av Gelb, Bruce D., Roberts, Amy E., Tartaglia, Marco

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Fgfr3 Is a Transcriptional Target of Ap2δ and Ash2l-Containing Histone Methyltransferase Complexes av Tan, Cheryl C., Walsh, Martin J., Gelb, Bruce D.

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Spacing Effect: SHP2 Phosphatase Regulates Resting Intervals Between Learning Trials in Long-Term Memory Induction av Pagani, Mario R., Oishi, Kimihiko, Gelb, Bruce D., Zhong, Yi

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Frequency of and Consequences of Aortic Dilation in Noonan Syndrome av Cornwall, James W., Green, Robert S., Nielsen, James C., Gelb, Bruce D.

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Noonan syndrome av Roberts, Amy E, Allanson, Judith E, Tartaglia, Marco, Gelb, Bruce D

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Genetics of Congenital Heart Disease: The Glass Half Empty av Fahed, Akl C., Gelb, Bruce D., Seidman, J. G., Seidman, Christine E.

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Biallelic loss-of-function variants in KCNJ16 presenting with hypokalemic metabolic acidosis av Webb, Bryn D., Hotchkiss, Hilary, Prasun, Pankaj, Gelb, Bruce D., Satlin, Lisa

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Signaling to Cardiac Hypertrophy: Insights from Human and Mouse RASopathies av Sala, Valentina, Gallo, Simona, Leo, Christian, Gatti, Stefano, Gelb, Bruce D, Crepaldi, Tiziana

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