- Home
- » Tags
- » Seckel syndrome
Top View
- Congenital Hand Anomalies and Associated Syndromes Ghazi M
- Utviklingsavvik V02
- 1 – Ust-Dzhegutinsky District; 2
- Classical Seckel Syndrome and Osteodysplastic Primordial Dwarfism Type Ii
- The University of Chicago Genetic Services Laboratories Labolaboratories 5841 S
- GENETIC TESTING REQUISITION Please Ship All NON-PRENATAL
- A Systems-Biology Approach to Understanding the Ciliopathy Disorders Ji Eun Lee and Joseph G Gleeson*
- WES Gene Package Intellectual Disability.Xlsx
- Neurodevelopment Next-Generation
- Aase–Smith Syndrome, 231 Abboud, M.R., 381 Abdallat Syndrome, 196
- T-Cell Clonality and Myelodysplasia Without Chromo- Somal Fragility in a Patient with Features of Seckel Syndrome
- Monogenic and Syndromic Obesity Precision Panel Overview Indications Clinical Utility
- Mackenzie's Mission Gene & Condition List
- Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
- GENETIC TESTING REQUISITION Please Ship All
- Blueprint Genetics Comprehensive Short Stature Syndrome Panel
- Genetic Syndromes Associated with Immune Abnormalities
- Blueprint Genetics Microcephaly and Pontocerebellar Hypoplasia Panel
- Seckel Syndrome: an Overdiagnosed Syndrome
- Overcoming the Limits of Rare Disease Matching Using Facial Phenotype Descriptors
- Genetic Evaluation of Proportionate Short Stature in Alexandria, Egypt
- Syndromic Disorders with Short Stature Zeynep Şıklar, Merih Berberoğlu Ankara University School of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey
- Diagnosed Cases of Rare Diseases at CENTOGENE January 2012 to June 2016
- Skin Disorders Panel Versie V4 (337 Genen) Centrum Voor Medische Genetica Gent
- Psykisk Utviklingshemming
- WES Gene Package Neuronal Migration Disorders.Xlsx
- WES Gene Package Multiple Congenital Anomalie
- Type 1 Established Condition List
- A Accessory Navicular Bone, 120–121 Accessory Ossicle, 143 Acetabulum
- Prevalence and Incidence of Rare Diseases: Bibliographic Data
- Prevalence and Incidence of Rare Diseases
- Atlas of Genetic Diagnosis and Counseling
- Fed Pract. 2020;37(Suppl 4):S82-S88. Doi:10.12788/Fp.0033 1 APC Familial Adenomatous Polyposis-1 AD Predisposition to Cancer
- Bone Dysplasias and Mental Functioning J
- Rare Diseases in Numbers
- Short Stature Precision Panel Overview Indications Clinical Utility
- OMIM Mendelian Gene List V2.0
- Orphanet Report Series Rare Diseases Collection
- Exome Sequencing Greatly Expedites the Progressive Research of Mendelian Diseases
- Recessive Gene List V2.0
- Genetic Diagnostics Test(S)/Gene(S)/Panel(S)
- Genetic Testing Requisition
- MACDP's Birth Defects and Genetic Diseases Branch 6-Digit Code
- Disease ID Disorder Name Gene Symbols OMIM ID