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- Tipping the Scales: Imbalances in Our Chromosomes April 28Th, 2021
- Burkitt Lymphoma and Ewing Sarcoma in a Child with Williams Syndrome
- Eurordis Summer School Alumni 2008 to 2015 By
- Orphanet Journal of Rare Diseases Biomed Central
- Genes & Chromosomes
- Parental and Chromosomal Origins of Microdeletion and Duplication Syndromes Involving 7Q11.23, 15Q11-Q13 and 22Q11
- Clinical Manifestations and Molecular Investigation of 50 Patients with Williams Syndrome in the Greek Population
- Autoimmune Diseases in Turner Syndrome ⁎ L
- Neoreviews Quiz
- Williams Syndrome
- 1 Curriculum Vitae Name: Anthony P
- Turner Syndrome and the Evolution of Human Sexual Dimorphism Bernard Crespi
- (To Access the Complete List of EURORDIS Members – Follow This Link
- Williams Syndrome: an Exploration of Neurocognitive and Genetic Features
- Williams Syndrome and Fragile X • Overview of Fragile X Syndrome
- Williams-Beuren Syndrome: Phenotypic Variability and Deletions of Chromosomes 7, 1 1, J Med Genet: First Published As 10.1136/Jmg.33.12.986 on 1 December 1996
- Title of Presentation Goes Here
- Williams Syndrome: Pediatric, Neurologic, and Cognitive Development
- The Principles of Clinical Cytogenetics
- Problem Behavior in Boys with Fragile X Syndrome
- Chromosome 7 Deregulation in Non-Small Cell Lung Carcinoma Molecular Landscape Evangelos Tsiambas1,6*, Vasileios Ragos2*, Alicia Y
- Abdominal Pain in Williams Syndrome, 205 Adderall, 96
- 7 Chromosome Chapter
- A Mother's Intuition and a Message for Physicians
- Multisystem Study of 20 Older Adults with Williams Syndrome Elizabeth M
- Burkitt Leukemia in a 5‑Year‑Old Girl with Williams–Beuren Syndrome: Review of the Literature
- Rare Disease Registries in Europe
- EURORDIS SUMMER SCHOOL ALUMNI 2008 to 2017
- What Is 22Q11.2 Deletion Syndrome? 22Q11.2 Deletion Syndrome Is a Genetic Condition That Affects Learning, Health, and Physical Traits
- Beuren Syndrome Associated Genes in Mouse Embryonic Stem Cells
- Constitutional and Somatic Deletions of the Williams-Beuren Syndrome Critical Region in Non-Hodgkin Lymphoma
- Digital Gene Expression Profiling Analysis of Childhood Acute Lymphoblastic Leukemia
- Fact Sheet for Mds: GI Concerns in Adults with Williams Syndrome
- Psychfeaturesinchildren.Pdf
- Epigenetics, Genomic Mutations and Cognitive Function Abraham Reichenberg a , Jonathan Mill B & James H
- 25, 1996, Sapporo, Japan
- Copy Number Variants at Williams–Beuren Syndrome 7Q11.23 Region
- Fragile X Syndrome Hydrocephalus
- Williams–Beuren Syndrome
- Burkitt Lymphoma and Williams Syndrome a Model for Children with a Multisystem Disorder and Malignancy
- Learning About Williams Syndrome
- Clinical Genetics (0141) 1.78
- Psychiatric Illness and Regression in Individuals with Phelan-Mcdermid Syndrome Teresa M
- Genetic Syndromes Websites
- Ameloblastoma in a Patient with Williams Syndrome and Use Of
- Genetic Disorders and Associated Behavioral Phenotypes
- High-Resolution Single Nucleotide Polymorphism Arrays Identified An
- Health Care Supervision for Children with Williams Syndrome Colleen A
- The Discovery of Microdeletion Syndromes in the Post-Genomic Era: Review of the Methodology and Characterization of a New 1Q41q42 Microdeletion Syndrome Lisa G
- Signs Indicating Dementia in Down, Williams and Fragile X Syndromes
- 7Q11.23 Duplication Syndrome
- The Genetics of Williams Syndrome: an Update
- Comparative Genomics of Autism and Schizophrenia
- Two High-Throughput Technologies to Detect Segmental Aneuploidies Identify New Williams-Beuren Syndrome Patients with Atypical Deletions
- Specific Disabilities and Their Impact on Sexual Expression
- Prevalence and Incidence of Rare Diseases
- Otitis Media in Yound Children with Disabilities—Practical Strategies
- Application of Molecular Genetics Techniques for Detecting Deleted Segmental Aneuploidy in Williams Syndrome Afaf Magbooli1*, Etimad Huwait2, Ibtessam R
- Genetic Syndromes Associated with Congenital Heart Disease Jung Min Ko, MD Department of Pediatrics, Seoul National University College of Medicine, Seoul, Korea
- ORD Resources Report
- Atypical Deletion of Williams-Beuren Syndrome Reveals the Mechanism of Neurodevelopmental Disorders
- Realizing the Potential of Behavioral Neurogenetics Research
- An Overview of Autism, Down Syndrome, Fragile X, Specific
- Overview of ADHD Symptoms in ID/D Laura Politte, M.D
- Constitutional and Somatic Deletions of the Williams