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1. Discordant clinical features of identical hypertrophic cardiomyopathy twins

2. Cells of the adult human heart

3. poly(UG)-tailed RNAs in genome protection and epigenetic inheritance

5. A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy

10. EM-mosaic detects mosaic point mutations that contribute to congenital heart disease

11. Different TBX5 Interactions in Heart and Limb Defined by Holt-Oram Syndrome Mutations

14. Robust identification of mosaic variants in congenital heart disease

21. Pathogenic variants damage cell compositions and single cell transcription in cardiomyopathies

23. Characterization of HPV and host genome interactions in primary head and neck cancers

24. Response to Brodehl et al.

25. Hypertrophic Cardiomyopathy

27. 515 Integrated analysis of acne identifies a critical role for immune fibroblastic cells (IFCs) in the pathophysiology of acne and in the action of isotretinoin

28. Ablation of lysophosphatidic acid receptor 1 attenuates hypertrophic cardiomyopathy in a mouse model

30. Spectrum of somatic mitochondrial mutations in five cancers

31. An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations

42. HEART DISEASE: Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy

43. Antibody Diversity

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