Syndactyly
Top View
- In an Inbred Kindred
- A Novel Single-Base Deletion in ROR2 Causes Atypical Brachydactyly Type B1 with Cutaneous Syndactyly in a Large Chinese Family
- Pierre Robin Syndrome
- A Guide to the Foot and Leg
- Brachydactyly and Syndactyly
- Fetal Anomalies of the Hands and Feet
- 7.1 Birth Defects Code List
- Craniosynostosis and Related Disorders Mark S
- Novel Autosomal Dominant Mandibulofacial Dysostosis with Ptosis: Clinical Description and Exclusion of TCOF1 P Hedera, H V Toriello, E M Petty
- Syndactyly and Desyndactyly
- Clinical and Genetic Characterization of Patients with Pierre Robin Sequence and Spinal Disease: Review of the Literature and Novel Terminal 10Q Deletion
- Craniosynostosis Syndromes Sequencing
- Syndactyly Repair with a Straight-Line Technique: a Case Series
- Review of X-Linked Syndromes with Arthrogryposis Or Early Contractures—Aid to Diagnosis and Pathway Identification Jesse M
- Blueprint Genetics Brachydactyly / Syndactyly Panel
- Craniosynostosis HAIDAR KABBANI, M.D., and TALKAD S
- Craniosynostosis and Syndactyly: Deletion Phenotype *
- Bilateral Ectrodactyly, Syndactyly with Split Foot Malformation in a Healthy