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Syndactyly
Genetics of Congenital Hand Anomalies
Massachusetts Birth Defects 2002-2003
Polydactyly of the Hand
Association of Syndactyly, Ectodermal Dysplasia, and Cleft Lip and Palate: Report of Two Sibs from Turkey
Identifying the Misshapen Head: Craniosynostosis and Related Disorders Mark S
Case Report Northern International Medical College Journal
14 Carpenter Syndrome
Natural History Study of Arthrogryposis Multiplex Congenita, Amyoplasia Type
Congenital Anomalies and in Utero Antiretroviral Exposure in Human Immunodeficiency Virus– Exposed Uninfected Infants
Association of Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy: the EEM Syndrome
BCOR Analysis in Patients with OFCD and Lenz Microphthalmia Syndromes, Mental Retardation with Ocular Anomalies, and Cardiac Laterality Defects
The Principles of Management of Congenital Anomalies of the Upper Limb
EUROCAT Syndrome Guide
Clinical Variability in Patients with Apert's Syndrome
Craniosynostosis
Fetal Micrognathia: Almost Always an Ominous Finding
Congenital Anomalies Associated with Cerebral Palsy and Mental Retardation by Ronald S
Genetic Hearing Loss- Syndromes
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
Ectrodactyly of the Foot
Pediatric Hand and Foot Surgery
Crouzon Syndrome
Congenital Hand Differences
Dubowitzsyndrome
Microtia: a Combined Approach by Genetics and Audiology
Limb Defects Sequencing Panel
Multiple Pterygium Syndrome*
Carpenter Syndrome—A Genetic Disease Dr
Jemds.Com Original Research Article
Syndrome Spotter Syndrome Spotter
Muscles and Bones in Charge Syndrome: Parent Information
Treacher Collins Syndrome (Mandibulofacial Dysostosis )
Orofacial Features of Treacher Collins Syndrome
Apert Syndrome --Pfeiffer Syndrome 22 A/V Strabismus A
Ectrodactyly/Split Hand Feet Malformation Case Report
12. Malformations of the Limbs and Extremities (J1-J7)
ARTHROGRYPOSIS Causes, Consequences And
Crouzon Syndrome - a Rare Genetic Disorder
Congenital Hand Anomalies - an Overview
Apert Syndrome