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Dolichostenomelia
Global Journal of Medical Research: F Diseases Cancer, Ophthalmology & Pediatric
Two Novel Pathogenic FBN1 Variations and Their Phenotypic Relationship of Marfan Syndrome
Abstracts from the 51St European Society of Human Genetics Conference: Electronic Posters
A Mutation in FBN1 Disrupts Profibrillin Processing and Results in Isolated Skeletal Features of the Marfan Syndrome Dianna M
Thoracic Cage Deformities in the Early Diagnosis of the Marfan Syndrome and Cardiovascular Disease
Prognosis Factors in Probands with an FBN1 Mutation Diagnosed Before the Age of 1 Year
A Case of Marfan Syndrome with Ascending and Arch of Aorta Aneurysm Presenting with Type A- Dissection of Aorta
00464 Genetic Testing for Marfan Syndrome
Proceedings Allergy, Asthma, Copd, Immunophysiology & Norehabilitology: Innovative Technologies
Skeletogenic Phenotype of Human Marfan Embryonic Stem Cells Faithfully Phenocopied by Patient-Specific Induced-Pluripotent Stem Cells
The Top 10 Dysmorphic Syndromes: Keys to Diagnosis/What's
ED368492.Pdf
2.04.129 Genetic Testing for Marfan Syndrome, Thoracic Aortic Aneurysms and Dissections, and Related Disorders Page 2 of 19
Differential Diagnosis
Guidelines for the Diagnosis and Manage...Cystathionine Beta
Neurocard 2017 Scientific Program & Book of Abstracts
A Case of Acute Paraplegia Due to Aortic Dissection in Marfan Syndrome
Abstracts from the 53Rd European Society of Human Genetics (ESHG) Conference: E-Posters
Top View
Genetic Disorders of Bone Or Osteodystrophies of Jaws—A Review
The Marfan Syndrome and Pregnancy: an Analysis of the Literature 39 3.1
Noninvasive Diagnosis and Management of Spontaneous
General Physical Examination for a Cardiovascular Patient
Genetic Testing for Marfan Syndrome, Thoracic Aortic Aneurysms and Dissections, and Related Disorders
Redalyc.Anthropometric and Musculoskeletal Assessment Of
Marfan's Syndrome: Natural History and Long-Term Follow-Up Of
Marfan's Syndrome: an Overview
FRACP Clinical Exam Notes
Anomalous Coronary Artery Origin in a Young Patient with Marfan Syndrome
Therapeutic and Diagnostic Agents
Mechanisms and Pathophysiology of Headache in the Population of Patients with Chiari Malformation and Hypermobility Connective Tissue Disorders
Acute Liver Failure Induced by Carbamazepine
The Marfan Syndrome and Related Phenotypes
Marfan Syndrome
Orthopaedic Management in Marfan Syndrome
Genetics Update for the Next Ration Clinician
Marfan Syndrome in Infancy – a Rare Condition with Poor Prognosis