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Brachydactyly
A Novel Locus for Brachydactyly Type A1 on Chromosome 5P13.3-P13.2 C M Armour, M E Mccready, a Baig,Agwhunter, D E Bulman
The Genetic Heterogeneity of Brachydactyly Type A1: Identifying the Molecular Pathways
Genetics of Congenital Hand Anomalies
Orphanet Journal of Rare Diseases Biomed Central
Craniofacial Development After Three Different Palatoplasties in Children Born with Isolated Cleft Palate
Blueprint Genetics Craniosynostosis Panel
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MR Imaging of Fetal Head and Neck Anomalies
IIA O B Dominant Trait
Robinow Syndrome M a Patton, a R Afzal
Identifying the Misshapen Head: Craniosynostosis and Related Disorders Mark S
Brachydactyly
Review Article Cleidocranial Dysplasia: Clinical and Molecular Genetics
Differential Diagnosis of Complex Conditions in Paleopathology: a Mutational Spectrum Approach by Elizabeth Lukashal a Thesis
A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita
Crouzono-Dermo-Skeletal Syndrome, Crouzon Syndrome with Acanthosis Nigricans Syndrome
Poland-Mobius Syndrome
EUROCAT Syndrome Guide
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Brachydactyly Type A1
Anaesthesia for a Child with Cleidocranial Dysplasia
Craniosynostosis
Dual Novel Mutations in SLC26A2 in Two Siblings with Multiple
25 Cleidocranial Dysplasia
Blueprint Genetics Arthrogryposes Panel
Genetic Syndromes Associated with Craniosynostosis
Brachydactyly and Polydactyly with Ridge Hypoplasia
Brachydactyly A-1 Mutations Restricted to the Central Region of the N-Terminal Active Fragment of Indian Hedgehog
Cystic Kidneys in a Patient with Craniofacial Abnormalities
(Multiple Congenital Contractures): Diagnostic Approach to Etiology, Classification, Genetics, and General Principles
A Rare Case of Poland's Syndrome
Cukurova Medical Journal Crouzon Syndrome in Two Siblings
Craniosynostosis Syndromes Sequencing
Mobius Syndrome with Poland's Anomaly*
Blueprint Genetics Micromelic Dysplasia Panel
Review of X-Linked Syndromes with Arthrogryposis Or Early Contractures—Aid to Diagnosis and Pathway Identification Jesse M
Blueprint Genetics Brachydactyly / Syndactyly Panel
Congenital Anonychia and Brachydactyly of the Left Foot-Cooks Syndrome Variant: Case Report and Review of Literature
The Characteristics of Craniofacial and Cervicovertebral Morphology in Different Genetic Syndromes - a Literature Review and Three Case Reports
Congenital Methemoglobinemia with Multiple Limb Anomalies in an 11-Year-Old
TGDS Pathogenic Variants Cause Catel‐Manzke Syndrome Without Hyperphalangy
Restorative Treatment Strategies for Patients with Cleidocranial Dysplasia
POLAND' SYNDROME: an Incidental Findings on Routine Medical Check
Microtia: a Combined Approach by Genetics and Audiology
The Evolution of the Role of Imaging in the Diagnosis of Craniosynostosis: a Narrative Review
Identifying Genetic Variants and Characterizing Their Role in Clubfoot
Poland Syndrome Coexisting with Blaschkolinear Congenital Melanocytic Nevi
Limb Defects Sequencing Panel
Cleidocranial Dysplasia: a Case Report
Jemds.Com Original Research Article
Controversies in Poland Syndrome: Alternative Diagnoses in Patients with Congenital Pectoral Muscle Deficiency
The Genetics of Isolated and Syndromic Clubfoot
Analysis of Variation in Clubfoot Candidate Genes
Arthrogryposis and Congenital Myasthenic Syndrome Precision Panel
BMPR1B Mutation Causes Pierre Robin Sequence
Rubinstein-Taybi Syndrome
Genetics of Craniosynostosis: Review of the Literature
Mobius Syndrome with Poland's Anomaly*
Poland's Syndrome with Spontaneous Pneumothorax: Report of Two Cases
Cleidocranial Dysplasia: Maxillary Alterations on the Transverse Plane. Presence of Crown-Radicular Anomalies and Multidisciplinary Approach of a Clinical Case
MACDP's Birth Defects and Genetic Diseases Branch 6-Digit Code