Robinow syndrome
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- Scott Syndrome (Faciogenital Dysplasia) – Update 2015
- Download PDF File
- Utviklingsavvik V02
- The Laboratory in the Multidisciplinary Diagnosis of Differences Or
- Connective Tissue Disorders
- 89 Robinow Syndrome R
- Anti-Müllerian Hormone: a Valuable Addition to the Toolbox of the Pediatric Endocrinologist
- Acrodysostosis : Autosomal Been Published in the Literature(1)
- Aase–Smith Syndrome, 231 Abboud, M.R., 381 Abdallat Syndrome, 196
- Syndromic and Nonsyndromic Systemic Associations of Congenital Lacrimal Drainage Anomalies: a Major Review
- Identification of Novel ROR2 Gene Mutations in Indian Children with Robinow Syndrome
- Blueprint Genetics Micromelic Dysplasia Panel
- ORPHA Number Disease Or Group of Diseases 300305 11P15.4
- Newborndxtm Advanced Sequencing Evaluation Disorders List
- Genetic Evaluation of Short Stature Laurie H
- Syndromic Disorders with Short Stature Zeynep Şıklar, Merih Berberoğlu Ankara University School of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey
- Diagnosed Cases of Rare Diseases at CENTOGENE January 2012 to June 2016
- Robinow Infosheet 6-14-19