DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Overgrowth syndrome
Overgrowth syndrome
Fetal Megacystis: a Lot More Than LUTO
Orphanet Report Series Rare Diseases Collection
With a Learning Disability; Guidance for General Practice
Craniosynostosis Precision Panel Overview Indications Clinical Utility
Chromosomal Microarray Analysis in Turkish Patients with Unexplained Developmental Delay and Intellectual Developmental Disorders
Statistical Analysis Plan
Omphalocele and Gastroschisis Precision Panel Overview Indications Clinical Utility
EUROCAT Syndrome Guide
Prenatal Microarray Disorders List V19.1
Syndromes and Constitutional Chromosomal Abnormalities
Genetic Mapping and Mutation Analysis of Genes Causing Human Hereditary Skeletal Disorders
Ocular Coloboma: a Reassessment in the Age of Molecular Neuroscience
Genetics and Metabolics Abbreviations and Diagnosis
Nuove Politiche Per L'innovazione Nel Settore Delle Scienze Della Vita
Abstracts from the 53Rd European Society of Human Genetics (ESHG) Conference: E-Posters
PI3K/Mtor Pathway Inhibition: Opportunities in Oncology and Rare Genetic Diseases
ORPHA Number Disease Or Group of Diseases 300305 11P15.4
Review of X-Linked Syndromes with Arthrogryposis Or Early Contractures—Aid to Diagnosis and Pathway Identification Jesse M
Top View
List Rare Diseases.Txt
Blueprint Genetics Macrocephaly / Overgrowth Syndrome Panel
Maldevelopment of the Human Kidney and Lower Urinary Tract: an Overview
Rare Disease Registries in Europe
Skin Disorders Panel Versie V4 (337 Genen) Centrum Voor Medische Genetica Gent
Fabio Pammolli, Massimo Riccaboni, Laura Magazzini, Mark Supekar
Maldevelopment of the Human Kidney and Lower Urinary Tract: an Overview
Congenital Anomalies – Case Studies and Mechanisms
Overgrowth Next Generation Sequencing (NGS) Panel: Rev 1.12 Information for Ordering Providers
Ventriculomegaly Precision Panel Overview Indications Clinical Utility
13Assessment of the Dysmorphic Infant
Variants in the Degron of AFF3 Cause a Multi-System Disorder With
Rare Disease Registries in Europe - June 2020 2
PTEN-Opathies: from Biological Insights to Evidence-Based Precision Medicine
Supplemental Data
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Prevalence and Incidence of Rare Diseases
Fed Pract. 2020;37(Suppl 4):S82-S88. Doi:10.12788/Fp.0033 1 APC Familial Adenomatous Polyposis-1 AD Predisposition to Cancer
Pituitary Gigantism Dr. Liliya Rostomyan
A Novel Microdeletion Syndrome at 3Q13.31 Characterised By
Orphanet Report Series Rare Diseases Collection
From Overgrowth Syndromes to Kidney Cysts