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Camptodactyly
Musculo-Contractural Ehlers-Danlos Syndrome
EUROCAT Syndrome Guide
Birth Defects Surveillance a Manual for Programme Managers
Beals Syndrome
Ocular Manifestations of Inherited Diseases Maya Eibschitz-Tsimhoni
Failure to Identify Antenatal Multiple Congenital Contractures and Fetal Akinesia – Proposal of Guidelines to Improve Diagnosis
Are Patients with Loeys-Dietz Syndrome Misdiagnosed with Beals Syndrome? Rebecca Woolnough, Andrew Dhawan, Kimberly Dow and Jagdeep S
Camptodactyly: Occurrence in Two New Genetic Syndromes and Its Relationship to Other Syndromes RICHARD M
Camptodactyly) J
Chromosome 1P36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings
(Multiple Congenital Contractures): Diagnostic Approach to Etiology, Classification, Genetics, and General Principles
7.1 Birth Defects Code List
Congenital Contractural Arachnodactyly
A New 1P36.13-1P36.12 Microdeletion Syndrome Characterized by Learning Disability, Behavioral Abnormalities, and Ptosis
Hereditary Disorders of Connective Tissue: a Guide to the Emerging Differential Diagnosis Maureen Murphy-Ryan, BS1, Apostolos Psychogios, MD2, and Noralane M
Review of X-Linked Syndromes with Arthrogryposis Or Early Contractures—Aid to Diagnosis and Pathway Identification Jesse M
Management of Simple Camptodactyly
ICD-10 Coding Manual List of All Reportable Congenital Malformations
Top View
Marfan's Syndrome: an Overview
Juvenile Type II Waardenburg Syndrome: a Rare Case Report in Kerala
Functional Genomic Analysis of Novel Microdeletions And
OEIS Complex Associated with Chromosome 1P36 Deletion: a Case Report and Review Ayman W
Congenital Contractural Arachnodactyly Suspected by Abnormally Long Extremities by Fetal Ultrasound Ryuta Miyake, Mayuko Ichikawa, Katsuhiko Naruse
EPHA4 Haploinsufficiency Is Responsible for the Short Stature of a Patient with 2Q35-Q36.2 Deletion and Waardenburg Syndrome
Identifying Candidate Genes for 2P15p16.1 Microdeletion Syndrome Using Clinical, Genomic, and Functional Analysis
Review Article Monosomy 1P36
Craniofacial Anomalies and Coding
MACDP's Birth Defects and Genetic Diseases Branch 6-Digit Code