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Clinodactyly
FROGLOG Newsletter of the Declining Amphibian Populations Task Force
Genetics of Congenital Hand Anomalies
CASE REPORT Radiographic Diagnosis of a Rare Case Of
A Progressive and Complex Clinical Course in Two Family Members With
Current Advances in Holt-Oram Syndrome Taosheng Huang, MD, Phd
Identifying the Misshapen Head: Craniosynostosis and Related Disorders Mark S
Craniofacial Diseases Caused by Defects in Intracellular Trafficking
Appendix 3.1 Birth Defects Descriptions for NBDPN Core, Recommended, and Extended Conditions Updated March 2017
Syndromes Affecting Ear Nose & Throat
Treatment Posibilities in Ectromelia
Hemimelia and Absence of the Peroneal Artery
EUROCAT Syndrome Guide
Choanal Atresia As a Feature of Ectrodactyly-Ectodermal Dysplasia
Hereditary Hearing Loss and It's Syndromes
Nager Acrofacial Dysostosis
Congenital Upper Limb Deformities Swanson's
Mutations in TFAP2B and Previously Unimplicated Genes of the BMP, Wnt, and Hedgehog Pathways in Syndromic Craniosynostosis
Excluded Conditions
Top View
Birth Defects Surveillance a Manual for Programme Managers
Pierre Robin Syndrome
Fetal Anomalies of the Hands and Feet
Guidelines for Conducting Birth Defects Surveillance
Clinical and Genetic Characterization of Patients with Pierre Robin Sequence and Spinal Disease: Review of the Literature and Novel Terminal 10Q Deletion
Aarskog's Syndrome
Craniosynostosis and Syndactyly: Deletion Phenotype *
Longitudinal Deficiency of Upper Limb: Similar Case Presentation of Two
Congenital Anomalies & Genetics
Ejhg201786.Pdf
Nager Acrofacial Dysostosis: Early
Title: Oral-Facial-Digital Syndrome Type 1 Genereview – Table 1 Authors
Pediatric Hand and Foot Surgery
TGDS Pathogenic Variants Cause Catel‐Manzke Syndrome Without Hyperphalangy
Dubowitzsyndrome
The Ontogeny of Robin Sequence
Postaxial Hypoplasia of the Lower Extremity in Children – Case Report
Clinodactyly Associated with Trisomy 21
Classification and Developmental Biology of Congenital Anomalies of the Hand and Upper Extremity Paul R
A Male Infant with the Catel-Manzke Syndrome and Dislocatable Knees Copyright
Congenital Anterolateral Tibial Bowing Associated with Polydactyly: Case Report and Literature Review
Audiology Clinical Practice Guideline Website Version Rev
Guideline for Care of Patients with the Diagnoses of Craniosynostosis: Working Group on Craniosynostosis
Original Article Novel HOXD13 Frameshift Mutation Causes Synpolydactyly and Clinodactyly
Thieme: Handbook of Pediatric Orthopedics
Rubinstein-Taybi Syndrome
Genetics of Craniosynostosis: Review of the Literature
Ventricular Septal Defect (VSD)
Severe Peripheral Joint Laxity Is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)-B4GALT7 and Spondylodysplastic-EDS-B3GALT6