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1دورية أكاديمية
المؤلفون: Russell, Bianca E, Rigueur, Diana, Weaver, Kathryn N, Sund, Kristen, Basil, Janet S, Hufnagel, Robert B, Prows, Cynthia A, Oestreich, Alan, Al‐Gazali, Lihadh, Hopkin, Robert J, Saal, Howard M, Lyons, Karen, Dauber, Andrew
المصدر: Molecular Genetics & Genomic Medicine. 7(11)
مصطلحات موضوعية: Biological Sciences, Genetics, Cardiovascular, Pediatric, Congenital Structural Anomalies, Heart Disease, 2.1 Biological and endogenous factors, Aetiology, Abnormalities, Multiple, Adult, Bone Diseases, Developmental, Bone Morphogenetic Protein Receptors, Type I, Cartilage, Craniofacial Abnormalities, Developmental Disabilities, Female, Homozygote, Humans, Infant, Intestinal Polyposis, Male, Muscular Atrophy, Mutation, Missense, Neoplastic Syndromes, Hereditary, Pedigree, Phenotype, Prognosis, atrial septal defect, BMP, bmpr1a protein, bone morphogenetic protein, human, Medicinal and Biomolecular Chemistry, Clinical Sciences, Medicinal and biomolecular chemistry
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/634681f4
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2دورية أكاديمية
المؤلفون: Basil, Janet S., Santoro, Stephanie L., Martin, Lisa J., Healy, Katherine Wusik, Chini, Barbara A., Saal, Howard M.
المصدر: In The Journal of Pediatrics June 2016 173:143-148