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- Genevista Fetal Dysmorphology: an Indispensable Tool for Synthesis Of
- Aase–Smith Syndrome, 231 Abboud, M.R., 381 Abdallat Syndrome, 196
- Nuove Politiche Per L'innovazione Nel Settore Delle Scienze Della Vita
- Mechanisms of Arterial Remodeling: Lessons from Genetic Diseases
- T Hart, BA, Gran, B., Weissert, R. EAE: Imperfect but Useful Models of Multiple Sclerosis. TRENDS in MOLECULAR MEDICINE 17(3
- Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the Babyseq Project
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- Ijcep0076955.Pdf
- WO 2016/069591 A2 6 May 2016 (06.05.2016) W P O P C T
- World Journal of Clinical Cases
- Keutel Syndrome: a Case Report with Aortic Calcification
- Ep 2188016 B1
- The Role of Secreted Phosphoprotein-24 in Osteoblast Differentiation and Matrix Mineralization
- Newborndxtm Advanced Sequencing Evaluation Disorders List
- Prevalence and Incidence of Rare Diseases: Bibilographic Data
- Diagnosed Cases of Rare Diseases at CENTOGENE January 2012 to June 2016
- Nosology and Classification of Genetic Skeletal Disorders
- Fabio Pammolli, Massimo Riccaboni, Laura Magazzini, Mark Supekar
- Centogene.Pdf
- Keutel Syndrome
- ZIEGLER-DISSERTATION-2018.Pdf
- Prevalence and Incidence of Rare Diseases: Bibliographic Data
- Prevalence and Incidence of Rare Diseases
- Fetal Chondrodysplasia Punctata Associated with Maternal Autoimmune Diseases: a Review
- Orphanet Report Series Rare Diseases Collection
- Recessive Gene List V2.0
- Saudi Patient with Keutel Syndrome, a Rare Disease Nouf Mohammed Aleid